Raras
Buscar doenças, sintomas, genes...
Atresia esofágica
ORPHA:1199CID-10 · Q39.1CID-11 · LB12.1OMIM 189960DOENÇA RARA

Doença esofágica congênita rara caracterizada por uma interrupção na continuidade do esôfago, com ou sem comunicação persistente com a traqueia. A apresentação clínica varia de acordo com a anatomia, podendo levar à incapacidade de engolir ou, nos casos mais graves, ao desconforto respiratório.

Mantido por Agente Raras·Colaborar como especialista →

Introdução

O que você precisa saber de cara

📋

Doença esofágica congênita rara caracterizada por uma interrupção na continuidade do esôfago, com ou sem comunicação persistente com a traqueia. A apresentação clínica varia de acordo com a anatomia, podendo levar à incapacidade de engolir ou, nos casos mais graves, ao desconforto respiratório.

Pesquisas ativas
11 ensaios
44 total registrados no ClinicalTrials.gov
Publicações científicas
4.175 artigos
Último publicado: 2026 Apr 15

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
1-5 / 10 000
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
0.0
Europe
Início
Neonatal
🏥
SUS: Cobertura mínimaScore: 35%
Centros em: PA, PR, SC, RS, ES +10CID-10: Q39.1
🇧🇷Dados SUS / DATASUS
PROCEDIMENTOS SIGTAP (5)
0202010503
Cariótipo — bandas G, Q ou Rgenetic_test
0202010600
Pesquisa de microdeleções/microduplicações por FISHlab_test
0202010694
Sequenciamento completo do exoma (WES)rehabilitation
0202010260
Dosagem de alfa-fetoproteína
0301070040
Atendimento em reabilitação — doenças raras
Você se identifica com essa condição?
O Raras está aqui pra te apoiar — com ou sem diagnóstico

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Entender a doença

Do básico ao detalhe, leia no seu ritmo

Preparando trilha educativa...

Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

🫃
Digestivo
12 sintomas
🫁
Pulmão
9 sintomas
🦴
Ossos e articulações
5 sintomas
😀
Face
4 sintomas
📏
Crescimento
4 sintomas
❤️
Coração
3 sintomas

+ 16 sintomas em outras categorias

Características mais comuns

90%prev.
Fístula traqueoesofágica
Muito frequente (99-80%)
55%prev.
Defeito ventilatório restritivo
Frequente (79-30%)
55%prev.
Bronquite
Frequente (79-30%)
55%prev.
Ausência de bolha gástrica na ultrassonografia fetal
Frequente (79-30%)
55%prev.
Déficit de crescimento na infância
Frequente (79-30%)
55%prev.
Aversão oral
Frequente (79-30%)
61sintomas
Muito frequente (1)
Frequente (14)
Ocasional (22)
Muito raro (23)
Sem dados (1)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 61 características clínicas mais associadas, ordenadas por frequência.

Fístula traqueoesofágicaTracheoesophageal fistula
Muito frequente (99-80%)90%
Defeito ventilatório restritivoRestrictive ventilatory defect
Frequente (79-30%)55%
BronquiteBronchitis
Frequente (79-30%)55%
Ausência de bolha gástrica na ultrassonografia fetalAbsence of stomach bubble on fetal sonography
Frequente (79-30%)55%
Déficit de crescimento na infânciaFailure to thrive in infancy
Frequente (79-30%)55%

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico4.175PubMed
Últimos 10 anos200publicações
Pico2025138 papers
Linha do tempo
2026Hoje · 2026🧪 2005Primeiro ensaio clínico📈 2025Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

🧬

Nenhum gene associado encontrado

Os dados genéticos desta condição ainda estão sendo catalogados.

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

Carregando...

Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Pipeline de tratamentos
Pipeline regulatório — de medicamentos já aprovados a drogas em pesquisa exploratória.
·Pré-clínico20
Medicamentos catalogadosEnsaios clínicos· 0 medicamentos · 20 ensaios
Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Atresia esofágica

Centros de Referência SUS

24 centros habilitados pelo SUS para Atresia esofágica

Centros para Atresia esofágica

Detalhes dos centros

Hospital Universitário Prof. Edgard Santos (HUPES)

R. Dr. Augusto Viana, s/n - Canela, Salvador - BA, 40110-060 · CNES 0003808

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital Infantil Albert Sabin

R. Tertuliano Sales, 544 - Vila União, Fortaleza - CE, 60410-794 · CNES 2407876

Serviço de Referência

Rota
Anomalias CongênitasDeficiência Intelectual

Hospital de Apoio de Brasília (HAB)

AENW 3 Lote A Setor Noroeste - Plano Piloto, Brasília - DF, 70684-831 · CNES 0010456

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Estadual Infantil e Maternidade Alzir Bernardino Alves (HIABA)

Av. Min. Salgado Filho, 918 - Soteco, Vila Velha - ES, 29106-010 · CNES 6631207

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital das Clínicas da UFG

Rua 235 QD. 68 Lote Área, Nº 285, s/nº - Setor Leste Universitário, Goiânia - GO, 74605-050 · CNES 2338424

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital Universitário da UFJF

R. Catulo Breviglieri, Bairro - s/n - Santa Catarina, Juiz de Fora - MG, 36036-110 · CNES 2297442

Atenção Especializada

Rota
Anomalias Congênitas

Hospital das Clínicas da UFMG

Av. Prof. Alfredo Balena, 110 - Santa Efigênia, Belo Horizonte - MG, 30130-100 · CNES 2280167

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Julio Müller (HUJM)

R. Luis Philippe Pereira Leite, s/n - Alvorada, Cuiabá - MT, 78048-902 · CNES 2726092

Atenção Especializada

Rota
Anomalias Congênitas

Hospital Universitário João de Barros Barreto

R. dos Mundurucus, 4487 - Guamá, Belém - PA, 66073-000 · CNES 2337878

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Lauro Wanderley (HULW)

R. Tabeliao Estanislau Eloy, 585 - Castelo Branco, João Pessoa - PB, 58050-585 · CNES 0002470

Atenção Especializada

Rota
Anomalias Congênitas

Instituto de Medicina Integral Prof. Fernando Figueira (IMIP)

R. dos Coelhos, 300 - Boa Vista, Recife - PE, 50070-902 · CNES 0000647

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Pequeno Príncipe

R. Des. Motta, 1070 - Água Verde, Curitiba - PR, 80250-060 · CNES 3143805

Serviço de Referência

Rota
Anomalias CongênitasDeficiência Intelectual

Hospital Universitário Regional de Maringá (HUM)

Av. Mandacaru, 1590 - Parque das Laranjeiras, Maringá - PR, 87083-240 · CNES 2216108

Atenção Especializada

Rota
Anomalias Congênitas

Hospital de Clínicas da UFPR

R. Gen. Carneiro, 181 - Alto da Glória, Curitiba - PR, 80060-900 · CNES 2364980

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Pedro Ernesto (HUPE-UERJ)

Blvd. 28 de Setembro, 77 - Vila Isabel, Rio de Janeiro - RJ, 20551-030 · CNES 2280221

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira (IFF/Fiocruz)

Av. Rui Barbosa, 716 - Flamengo, Rio de Janeiro - RJ, 22250-020 · CNES 2269988

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital São Lucas da PUCRS

Av. Ipiranga, 6690 - Jardim Botânico, Porto Alegre - RS, 90610-000 · CNES 2232928

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital de Clínicas de Porto Alegre (HCPA)

Rua Ramiro Barcelos, 2350 Bloco A - Av. Protásio Alves, 211 - Bloco B e C - Santa Cecília, Porto Alegre - RS, 90035-903 · CNES 2237601

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário da UFSC (HU-UFSC)

R. Profa. Maria Flora Pausewang - Trindade, Florianópolis - SC, 88036-800 · CNES 2560356

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital das Clínicas da FMUSP

R. Dr. Ovídio Pires de Campos, 225 - Cerqueira César, São Paulo - SP, 05403-010 · CNES 2077485

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Base de São José do Rio Preto

Av. Brg. Faria Lima, 5544 - Vila Sao Jose, São José do Rio Preto - SP, 15090-000 · CNES 2079798

Atenção Especializada

Rota
Anomalias Congênitas

Hospital de Clínicas da UNICAMP

R. Vital Brasil, 251 - Cidade Universitária, Campinas - SP, 13083-888 · CNES 2748223

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Clínicas de Ribeirão Preto (HCRP-USP)

R. Ten. Catão Roxo, 3900 - Vila Monte Alegre, Ribeirão Preto - SP, 14015-010 · CNES 2082187

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

UNIFESP / Hospital São Paulo

R. Napoleão de Barros, 715 - Vila Clementino, São Paulo - SP, 04024-002 · CNES 2688689

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo
Sobre os centros SUS: Estes centros são habilitados pelo Ministério da Saúde como Serviços de Referência em Doenças Raras ou Serviços de Atenção Especializada. O atendimento é pelo SUS, com encaminhamento da rede de atenção básica.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

🟢 Recrutando agora

8 pesquisas recrutando participantes. Converse com seu médico sobre a possibilidade de participar.

Outros ensaios clínicos

44 ensaios clínicos encontrados, 11 ativos.

Distribuição por fase
Ver todos no ClinicalTrials.gov
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Publicações mais relevantes

Timeline de publicações
1.711 papers (10 anos)

Mostrando amostra de 200 publicações de um total de 1.711

#1

Stricture classification of pediatric esophageal strictures (SCOPES): A novel tool to predict response to endoscopic therapy.

Journal of pediatric gastroenterology and nutrition2026 Mar 23

Esophageal anastomotic stricture is a common complication following esophageal atresia (EA) repair. While multiple endoscopic therapies exist, predicting individual stricture response remains challenging. Existing classification systems focus primarily on luminal diameter and do not account for complex physical characteristics of the stricture. We developed and evaluated a novel endoscopic scoring tool, stricture classification of pediatric esophageal strictures (SCOPES), to determine if physical features are predictive of treatment response. In addition to its predictive utility, SCOPES aims to standardize the description of and improve communication of stricture morphology across providers and institutions. A retrospective cohort study was conducted on EA patients treated at a tertiary referral center between 2019 and 2024. Patients with ≥2 endoscopies and documented SCOPES scores were included. The SCOPES tool categorizes strictures based on diameter, length, scar band intrusion, symmetry, and presence of diverticula. Multivariable mixed-effects regression models were used to analyze associations between SCOPES characteristics and the primary outcome of number of therapeutic endoscopies within 6 months. Seventy patients (238 endoscopies) met inclusion criteria. In multivariable analysis, symmetric strictures and those with highly intrusive scar bands were significantly associated with a greater number of therapeutic endoscopies within 6 months. Two complications were observed, both managed without long-term sequelae. The SCOPES classification tool identifies physical stricture features that significantly influence response to endoscopic therapy. Circumferential symmetry and scar tissue protuberance were associated with higher treatment burden, suggesting these characteristics may guide therapeutic decision-making. SCOPES may aid in individualizing endoscopic management of pediatric esophageal strictures and warrants prospective validation.

#2

Neurodevelopmental assessment at 24 months in infants with esophageal atresia: A prospective cohort study.

Journal of pediatric gastroenterology and nutrition2026 Mar 19

To evaluate neurodevelopment at 24 months in infants surgically treated for esophageal atresia (EA), using the ages and stages questionnaire (ASQ), and identify perinatal and early-life factors associated with developmental delay. Infants with EA were prospectively enrolled in a structured multidisciplinary follow-up program. Total ASQ scores ≤185 were considered indicative of significant neurodevelopmental delay, while scores >220 reflected reassuring neurodevelopment. Five skill domains (communication, gross motor skills, fine motor skills, problem solving, and social skills) were also assessed. Clinical, surgical, and growth data were analyzed to identify associated risk factors. Of the 74 infants included, 13 patients (18%) had an ASQ score ≤185. Lower ASQ scores were significantly associated with prematurity, prolonged hospitalization, multiple surgeries, poor weight gain at 1 and 2 years, and feeding disorders. After adjusting for gestational age and genetic anomalies, prolonged hospitalization remained associated with lower ASQ scores, and higher weight-for-age at 1 and 2 years with better ASQ scores. Communication and social skills were the most severely affected, with approximately 80% of infants in the ASQ ≤ 185 group scoring below -2 standard deviations. Although most children with EA demonstrated normal development at 2 years, a minority experienced significant delays, especially in communication and social skills. Early screening and targeted multidisciplinary follow-up are essential to support optimal outcomes in this high-risk population.

#3

Induced Pluripotent Stem Cells as a Tool to Decipher the Normal and Abnormal Development of the Esophagus and Trachea from Normal Morphogenesis to Esophageal Atresia, Tracheomalacia, and Laryngo-Tracheal Clefts.

Cells2026 Mar 03

The development of the esophagus and trachea following the septation of the anterior foregut is a highly regulated process involving bidirectional communication between the endoderm and mesoderm. Signaling pathways such as the Bone Morphogenetic Protein family, Wnt/β-catenin, Sonic Hedgehog, and Fibroblast Growth Factor family mediate this complex crosstalk to induce the dorsal-ventral patterning of the anterior foregut as well as lineage specification. Even though the mechanisms are not fully understood, dysregulation of signaling pathways may lead to congenital malformations such as tracheomalacia, laryngeal-tracheal clefts and multiple types of esophageal atresia with/without tracheoesophageal fistula (EA/TEF). Human induced pluripotent stem cells (iPSCs) provide a robust in vitro platform to monitor the normal and abnormal development of esophagus and trachea and to understand the roles of the endoderm and mesoderm during anterior foregut development. Recent studies have demonstrated that direct differentiation of iPSCs into epithelial and mesenchymal lineages can recapitulate the key stages of foregut development. In this regard, in the current paper, we review the signaling pathways involved in the development of organs deriving from the anterior foregut as well as the roles of the endoderm and mesoderm revealed by previous studies. Furthermore, we discuss the use of iPSCs as a valuable model for investigating the bidirectional communications between the endoderm and mesoderm, which can broaden our knowledge and understanding of the critical mechanisms leading to normal and abnormal development of the esophagus and trachea.

#4

Risk factors for anastomotic complications following thoracoscopic repair of type III esophageal atresia in neonates: a single-center retrospective cohort study.

Frontiers in pediatrics2026

Although thoracoscopic repair in China has emerged as a preferred and increasingly adopted minimally invasive approach for esophageal atresia (EA), anastomotic complications remain a major concern, with reported incidences ranging from 15% to 80%. However, the independent risk factors for these complications in a homogeneous surgical population remain poorly characterized. This single-center retrospective cohort study recruited neonates with type III EA who underwent primary thoracoscopic repair. Comprehensive demographic, operative, and anatomic variables were gathered. Univariate and multivariable logistic regression analyses were utilized to identify independent predictors for anastomotic leak (AL), anastomotic stricture (AS), and recurrent tracheoesophageal fistula (recurrent TEF). The cohort had a mean birth weight of 2,597 g and a median operative time of 2.3 h. The incidences of AL, AS, and recurrent TEF were 15.4%, 74.6%, and 6.5%, respectively. Multivariable analysis identified distinct etiological mechanisms: an operative time of ≤2 h independently protected against AL (OR 0.24, 95% CI 0.09-0.63); the institutional learning curve attenuated traditional AS risk factors such as low birth weight; and the presence of a respiratory anomaly was the strongest predictor of recurrent TEF (OR = 8.84; 95% CI, 2.09-33.47). Minimal co-occurrence among the three complications (phi coefficients ≈ 0) confirmed their etiological independence. The three major anastomotic complications of thoracoscopic EA repair stem from distinct mechanisms. Anastomotic leak was independently protected by operative time ≤2 h (OR 0.24, 95% CI 0.09-0.63). The institutional learning curve attenuated traditional risk factors for anastomotic stricture (incidence 74.6%). Recurrent TEF was predominantly associated with respiratory anomalies (OR 8.84, 95% CI 2.09-33.47). This highlights the need for precision-based management. The robustness of these key associations was further confirmed through sensitivity analyses and enhanced methodological rigor, including assessments of predictor correlations and model diagnostics.

#5

Development of a lifelong core outcome set for oesophageal atresia ± tracheoesophageal fistula: the OCELOT study.

BMJ open2026 Mar 04

Despite anatomical correction, people born with oesophageal atresia±tracheoesophageal fistula (OA-TOF) experience lifelong morbidity. Core outcome sets (COSs) are recognised as a means of improving research quality and, as a consequence, improving patient outcomes; one was not available for this population. The scope of the study was to develop a COS for people born with OA-TOF that would be applicable regardless of age or geographic location. Patient input was paramount to this study. For long-list generation, in addition to the systematic review (SR), patients and representatives were invited to participate in focus groups, interviews or complete activity packs to ascertain outcomes that matter most to them. International consensus was then sought using a two-step Delphi survey followed by an online consensus meeting. Eight outcomes were identified through patient events that had not been picked up from SR. 175 people completed the Delphi survey from 26 countries and health care professionals from 13 different disciplines. 24 outcomes met predefined criteria for inclusion and following discussion and voting in the consensus meeting, and 14/24 outcomes were agreed for inclusion in the COS. 14 outcomes have been agreed on to form the COS. 12 of these outcomes are relevant to people of all ages, 1 to paediatric population and 1 to adult cohorts. The COS is, therefore, truly applicable lifelong, which was the scope of the project. This COS will help reduce research heterogeneity, enabling better quality research outcomes and more comparable data.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC2.795 artigos no totalmostrando 195

2026

Revisiting Fundoplication in Esophageal Atresia: Implications for Nutrition, Stricture Management, and Wrap Type.

Journal of pediatric surgery
2026

VACTERL Association in Screened Patients with Esophageal Atresia: A Retrospective Cohort Study.

Journal of pediatric surgery
2026

Stricture classification of pediatric esophageal strictures (SCOPES): A novel tool to predict response to endoscopic therapy.

Journal of pediatric gastroenterology and nutrition
2026

"It's a journey": Psychosocial perspectives on parenting a young child with esophageal atresia.

Pediatric surgery international
2026

Neurodevelopmental assessment at 24 months in infants with esophageal atresia: A prospective cohort study.

Journal of pediatric gastroenterology and nutrition
2026

Evaluation of surgical outcomes of thoracoscopic esophageal atresia repair with and without preservation of azygos vein: a retrospective cohort study.

Pediatric surgery international
2026

Overcoming the learning curve: a pictorial journey through technical adaptations for thoracoscopic esophageal atresia/tracheoesophageal fistula repair.

Indian journal of thoracic and cardiovascular surgery
2026

Induced Pluripotent Stem Cells as a Tool to Decipher the Normal and Abnormal Development of the Esophagus and Trachea from Normal Morphogenesis to Esophageal Atresia, Tracheomalacia, and Laryngo-Tracheal Clefts.

Cells
2026

Endoscopic puncture and recanalization in a child with corrosive esophageal stenosis and atresia: case report and literature review.

BMC pediatrics
2026

Is there any difference between surgical and endoscopic interventions related to the outcome of recurrent tracheoesophageal fistulas? A systematic review.

Journal of pediatric surgery
2026

Portable Neonatal Esophageal Atresia Simulator Improves MIS Acquisition Amongst Surgical Trainees: A Randomized Control Crossover Trial.

Journal of laparoendoscopic &amp; advanced surgical techniques. Part A
2026

Usefulness of Transparent Illumination Device in Esophageal Atresia for the Detection of the Distal Esophagus.

Surgical case reports
2026

Progression of esophageal atresia associated Barrett's esophagus in adulthood - Is endoscopic surveillance worth it?

Journal of pediatric surgery
2026

Management of postoperative leaks and infections in patients with esophageal atresia.

Seminars in pediatric surgery
2026

Risk factors for anastomotic complications following thoracoscopic repair of type III esophageal atresia in neonates: a single-center retrospective cohort study.

Frontiers in pediatrics
2026

Development of a lifelong core outcome set for oesophageal atresia ± tracheoesophageal fistula: the OCELOT study.

BMJ open
2026

Thoracoscopic staged repair for type A and type B esophageal atresia: outcomes from a tertiary center.

Pediatric surgery international
2026

Parents' experiences of condition management in children born with esophageal atresia-tracheoesophageal fistula during their early childhood.

Orphanet journal of rare diseases
2026

Comparison of outcomes between thoracostomy and non-thoracostomy management in patients undergoing esophageal atresia surgery: a retrospective study in a tertiary care center (2018-2021).

Journal of cardiothoracic surgery
2026

A Novel Association Between Mandibulofacial Dysostosis with Microcephaly and Congenital Diaphragmatic Hernia.

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
2026

Fiber-Guided Red Light-Emitting Diode Localization of an Esophageal Blind End in Long-Gap Esophageal Atresia Surgery: A Case Report.

Surgical case reports
2026

Biodegradable and self-expanding metal stents in the treatment of children with strictures after esophageal atresia repair.

Esophagus : official journal of the Japan Esophageal Society
2026

Peroral endoscopic tunneling stricturotomy for diverticulum treatment: novel procedure for pediatric esophageal anastomotic diverticula.

VideoGIE : an official video journal of the American Society for Gastrointestinal Endoscopy
2026

A Rare Dual Atresia Case Report Introducing Gastric Distension-Assisted Esophageal Approximation (GDEA): A Hypothetical Novel Technique for Long-Gap Esophageal Atresia.

International medical case reports journal
2026

Pediatric Quality of Life Post Esophageal Atresia Repair: A Systematic Review and Meta-Analysis.

Journal of pediatric surgery
2026

Gender Equity in pediatric surgical care in Central and South Asia: A systematic review and meta-analysis.

Journal of pediatric surgery
2026

Implementation and Evaluation of a Protocol for the Management of Type C Tracheoesophageal Fistula.

The Journal of surgical research
2026

Perioperative Care for Pediatric Patients Undergoing Lung Surgery: Retrospective Single Center Review.

Paediatric anaesthesia
2026

The power of pretend: Caregiver perspectives on sham feeding for infants with long-gap esophageal atresia.

Journal of pediatric surgery
2026

Profibrotic Changes Following Tension Application in a Fetal Lamb Model of Long Gap Esophageal Atresia.

bioRxiv : the preprint server for biology
2026

Eosinophilic esophagitis after tracheoesophageal fistula repair.

Journal of pediatric surgery
2026

Robotic-assisted posterior tracheopexy (RAPT), a minimal invasive approach to treat severe trachobroncomalacia: A retrospective single center experience.

Journal of pediatric surgery
2026

A call for personalized transition of care in congenital surgical anomalies: A population-based cohort study on healthcare utilization from birth to adulthood.

Journal of pediatric surgery
2026

Postoperative evaluation of esophageal atresia: consistency between multichannel intraluminal impedance pH measurements and endoscopic findings.

Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus
2025

Outcomes of Thoracic Surgery in Pediatric Patients: A Single-Center Experience From Al Ribat University Hospital, Sudan.

Cureus
2025

Successful treatment of corrosive esophageal atresia in a child using combined antegrade-retrograde dilation: a case report.

Frontiers in pediatrics
2026

Neonatal surgical mortality in East Africa: A systematic review and meta-analysis.

Journal of pediatric surgery
2026

Revisiting Turkish Esophageal Atresia Regisrty data for quality indicators.

Journal of pediatric surgery
2026

Membranous esophageal atresia without tracheoesophageal fistula in a neonate: a rare case report and literature review.

BMC pediatrics
2026

Evolving Surgical Practices in Esophageal Atresia: Insights from the EUPSA-ERNICA Survey a Decade After the 2014 Baseline Study.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
2026

Incidence of Esophageal Atresia and Associated Respiratory Morbidity in Children: A National Registry Study in Denmark (1998-2018).

Pediatric pulmonology
2026

Impact of Azygos Vein Preservation on Postoperative Outcomes in Esophageal Atresia: A Systematic Review and Meta-Analysis from the Pediatric Surgery Meta-Analysis (PESMA) Study Group.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
2026

Risk factors for 30-day mortality following major neonatal surgery: insights from a 10-year cohort in southern Tunisia.

Surgery today
2026

The role of contrast-enhanced ultrasound in the diagnosis of gastroesophageal reflux.

Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica
2026

Preservation of the azygos vein versus ligation of the azygos vein during surgical repair of esophageal atresia-tracheoesophageal fistula-a systematic review and meta-analysis.

Journal of pediatric surgery
2026

Feeding difficulties in children with esophageal atresia: A parent-reported multicenter study.

Journal of pediatric gastroenterology and nutrition
2025

Esophageal atresia with and without tracheoesophageal fistula: a 2016-2024 single-center cohort study in Saudi Arabia stratified by gap length.

World journal of pediatric surgery
2026

Health Care-Associated Infections following Major Neonatal Surgery in a Resource-Limited Setting: Risk Factors and Outcomes from Southern Tunisia.

American journal of perinatology
2026

Comparison of esophageal atresia with and without VACTERL association: A retrospective study.

Pediatrics international : official journal of the Japan Pediatric Society
2025

Tracheobronchial Membrane Tapering Resection for Tracheobronchomalacia With Wide Posterior Membrane.

The Annals of thoracic surgery
2026

Endoscopic tracheoesophageal fistula closure-Electrocautery combined with esophageal clip application in pediatric patients.

Journal of pediatric gastroenterology and nutrition
2025

Invited Commentary on: Outcomes After Open Thoracotomy Repair of Esophageal Atresia with or Without Tracheoesophageal Fistula: A 10-Year Middle Eastern Multicenter Retrospective Cohort.

Journal of pediatric surgery
2025

Laparoscopic gastrostomy insertion for long gap oesophageal atresia in newborn babies.

Pediatric surgery international
2025

The role of simulation in mastering highly specialized pediatric surgery: current trends and future perspectives.

Innovative surgical sciences
2026

Gastro-Esophageal Reflux in Esophageal Atresia Patients Remains a Challenge: Results from a Systematic Review and Meta-Analysis.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
2025

Esophageal Atresia: From worry to wisdom-Parental information needs and considerations on etiology, care, and parental support.

Global pediatrics
2025

Diagnostic and surgical challenges in atypical forms of esophageal atresia: A case series.

Pediatrics and neonatology
2025

Esophageal Atresia, an Anomaly of VACTERL Association or Novel Feature of the FGF10 Gene: A Case Report.

Molecular syndromology
2025

Outcomes after open thoracotomy repair of esophageal atresia with or without tracheoesophageal fistula: A 10-year middle eastern multicenter retrospective cohort.

Journal of pediatric surgery
2025

Association Between Congenital Gastrointestinal Malformation Outcome and Largely Asymptomatic SARS-CoV-2 Infection in Pediatric Patients-A Systematic Review.

Journal of clinical medicine
2025

TRACHEOESOPHAGEAL FISTULA WITH ESOPHAGEAL ATRESIA IN QASSIM REGION: EPIDEMIOLOGY, CLINICAL CHARACTERISTICS AND OUTCOMES, A RETROSPECTIVE STUDY.

Georgian medical news
2025

Late Manifestation of Invasive Adenocarcinoma in a Right-Colon Interposition for Esophageal Atresia.

Cureus
2025

Adults following open esophageal atresia repair: evaluating long-term musculoskeletal and pulmonary outcomes using insights from real-time MRI.

Pediatric research
2025

Long-term outcomes after colon interposition for esophageal replacement: a case series of four patients from a single centre.

The Pan African medical journal
2025

Surgical repair of esophageal atresia: do trans-anastomotic feeding tubes have an impact on the outcome?

Frontiers in pediatrics
2026

Outcomes of various surgical approaches to long-gap esophageal atresia: A systematic review and meta-analysis.

Journal of pediatric surgery
2025

Fogarty Catheter Placement for Subglottic H-Type Tracheoesophageal Fistula via a Supraglottic Airway: A Case Report.

Case reports in pediatrics
2025

Diagnosis, Treatment, and Follow-Up of Tracheo/Bronchomalacia in Children: The Italian Multicenter Experience.

Children (Basel, Switzerland)
2025

Long-Term Bladder Dysfunction and Bilateral Obstructive Megaureter in VACTERL Syndrome: A Case Report of Challenging Urological Management.

Reports (MDPI)
2025

Comparative analysis of outcomes of one stage versus staged surgical repair in esophageal atresia: an audit from a tertiary pediatric center in low resources country.

BMC surgery
2026

Aerodigestive Clinic: Multidisciplinary Follow Up for Oesophageal Atresia and Tracheoesophageal Fistula Patients.

Journal of paediatrics and child health
2025

Outcomes of Esophageal Atresia at University Tertiary Hospital of Kigali, Rwanda.

Research square
2026

Diversion pharyngostomy: A new surgical technique to manage salivary aspiration associated with complete esophageal stenosis.

Journal of pediatric surgery
2026

Nerve injury and vocal cord paralysis after esophageal atresia and tracheoesophageal fistula repair: Systematic review and meta-analysis.

Journal of pediatric surgery
2025

Thoracoscopic management of recurrent tracheoesophageal fistula: a single-center outcome analysis.

BMC surgery
2025

Regenerative reconstruction of mature esophageal epithelium by engraftment of esophageal organoids in de-epithelialized mouse colon.

Pediatric surgery international
2025

Atresia at the gastroesophageal junction associated with left congenital diaphragmatic hernia: a diagnostic and surgical challenge.

BMJ case reports
2025

Case Report: Unveiling CHARGE syndrome: a neonatal case study with esophageal atresia and feeding difficulties.

Frontiers in pediatrics
2025

Iatrogenic Esophageal Perforation in Extremely Premature Babies With Low Birth Weight: A Case Series at a Single Tertiary-Care Center.

Cureus
2025

Clinical characteristics and treatment outcomes of pediatric achalasia: a 10-year experience from a tertiary center in Iran.

BMC research notes
2025

Esophageal atresia with concomitant hypertrophic pyloric stenosis: a case series and literature review.

BMC pediatrics
2025

Evaluation of food intake, malnutrition, growth and development in children with esophageal atresia: a pilot study from Turkey.

BMC pediatrics
2026

Assisted reproductive technology and esophageal atresia: Dangerous liaisons?

Journal of pediatric surgery
2025

Current status of neonatal surgery in Japan: An analysis of data from the National Clinical Database Pediatric Surgical Registry.

Pediatric surgery international
2025

Whole-Exome Sequencing Revealed a Novel De Novo Pathogenic EFTUD2 Variant in Mandibulofacial Dysostosis, Guion-Almeida Type: Reinforcing Links to Choanal and Oesophageal Atresia.

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
2025

Beyond the Usual: A Rare Case of Tracheoesophageal Fistula.

Cureus
2025

Prenatal diagnosis and outcome of meso/dextrocardia: a single-center report of 29 cases.

Journal of medical ultrasonics (2001)
2025

Case Report of Neonatal Bronchoesophageal Fistula With Esophageal Atresia.

A&amp;A practice
2025

Outcomes and challenges in the management of esophageal atresia and/or tracheoesophageal fistula: insights from Turkish Esophageal Atresia Registry.

World journal of pediatric surgery
2025

Diagnosis of Lissencephaly in a Neonate After Antenatal Polyhydramnios and Suspicion of Fetal Esophageal Atresia: A Case Report.

Cureus
2026

High-volume hospitals experience fewer postoperative complications after neonatal surgery: Analyses of the National Clinical Database Pediatric Surgical Registry in Japan.

Journal of pediatric surgery
2026

Retrospective case-control study of nutritional and respiratory status in children with type III esophageal atresia.

Journal of pediatric gastroenterology and nutrition
2025

Interdisciplinary transition of care for congenital gastrointestinal malformations: analysis of a standardized program.

International journal of adolescent medicine and health
2025

Complications of thoracoscopic TEF clipping for fistula ligation: a case report of polymer clip migration into the right main bronchus and recurrent fistula.

Frontiers in pediatrics
2025

Nutritional status and surgical outcomes in patients with esophageal atresia: findings from Turkish Esophageal Atresia Registry.

Pediatric surgery international
2025

Operating Without Direct Supervision During Pediatric Surgery Fellowship: When, How, and Why?

Journal of pediatric surgery
2025

Long term functional outcomes and health-related quality of life in patients with esophageal atresia - A tertiary centre experience.

Journal of pediatric surgery
2025

Esophageal Atresia and Intrathoracic Stomach in a Complex Case of Congenital Anomalies.

Children (Basel, Switzerland)
2025

Persistent Low-Output Neonatal Chylothorax: How Long Are We Justified to Wait for Pleurodesis in Partial Responders?

Pediatric pulmonology
2025

Impact of VACTERL Association and Chromosomal Anomalies on Outcomes After Esophageal Atresia Repair: Insights from the EUPSA Registry.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
2025

Cardiovascular Anomalies Associated With Esophageal Atresia: A 23-Year Single-Center Experience.

Cureus
2025

Challenges of Long-Gap Esophageal Atresia Repair in a Patient With Tetralogy of Fallot and Right Aortic Arch.

Cureus
2025

Cholecystohepatic duct (type IIIA) - fifth report of aberrant biliary pathology in a paediatric case of oesophageal atresia and imperforate anus with review of literature.

Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology
2025

Risk factors for 30-day mortality in neonates undergoing surgery for esophageal atresia.

Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus
2025

Outcome of Esophageal Atresia: What Choice of Suture Material?

Journal of pediatric surgery
2025

Thoracoscopic internal traction for long-gap esophageal atresia: outcomes, challenges, and complications.

Pediatric surgery international
2025

Conservative Management of Anastomotic Leak after Repair of Type C Esophageal Atresia: A Retrospective Audit.

Journal of Indian Association of Pediatric Surgeons
2025

Failed Extubation After Primary Repair of Type C Esophageal Atresia: Frequency and Risk Factors.

Journal of pediatric surgery
2025

Does assisted reproductive technology influence the complexity and associated malformations in esophageal atresia?

Journal of assisted reproduction and genetics
2025

Risk Factors for Nosocomial Infections Following Surgical Repair of Esophageal Atresia.

World journal of surgery
2025

Thoracoscopic versus conventional thoracotomy for esophageal atresia/tracheoesophageal fistula repair: a comprehensive meta-analysis of 25 comparative studies.

Pediatric surgery international
2025

Tracheal Work of Breathing in Neonates With Tracheoesophageal Fistula Before and After Surgical Repair via Computational Fluid Dynamics Assessment.

Journal of pediatric surgery
2025

Comprehensive Insights into Tracheoesophageal Fistula Pathophysiology, Diagnosis, Treatment, and Future Directions.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
2025

Benefits and barriers to using a portable thoracoscopic esophageal atresia simulator as perceived by surgical trainees.

Pediatric surgery international
2026

Primary posterior tracheopexy in esophageal atresia with tracheomalacia: From innovation to multicenter RCT.

Journal of pediatric surgery
2025

Risk Factors Associated with Early and Late Postoperative Complications in Neonatal Patients with Esophageal Atresia.

Children (Basel, Switzerland)
2026

Impact and Citation Trends of Surveys Endorsed by the EUPSA Network Office in Pediatric Surgery: A Bibliometric Analysis.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
2025

Oesophageal dilatation for the anastomotic stricture post trachea-oesophageal fistula/oesophageal atresia repair.

Pediatric surgery international
2026

Esophageal Atresia Repair in Germany: Utilization Patterns, Hospital Characteristics and Costs.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
2025

Internal traction as an effective bridge to successful anastomosis in complex esophageal atresia.

Journal of pediatric surgery
2025

Long-Term Nutritional Status in Children Born With Esophageal Atresia.

Pediatrics
2025

Experiences of symptom burden among young children born with esophageal atresia-tracheoesophageal fistula: a US focus group study.

Orphanet journal of rare diseases
2025

Letter: Can We Predict Post-Operative Sepsis in Neonates Undergoing Surgery for Esophageal Atresia?

Surgical infections
2025

Refractory Bradycardia and Unreactive Mydriasis Revealing Severe Intraoperative Neonatal Hypothermia in a Resource-Limited Setting.

Cureus
2025

A Comparative Study of the Clinical Characteristics of Esophageal-Pulmonary Fistula in Children.

Journal of pediatric surgery
2025

Endoscopic remodeling of esophageal stenosis refractory to traditional endoscopic treatment.

JPGN reports
2025

Endoscopic Treatment of Very-Delayed-Onset Tracheoesophageal and Esophagocutaneous Fistulae after Colonic Interposition for Esophageal Atresia.

ACG case reports journal
2026

Prenatal diagnosis of esophageal atresia - Still a challenge.

Journal of pediatric surgery
2025

Delayed diagnosis of isolated congenital H-type tracheoesophageal fistula: a case report of surgical repair supported by TachoSil® as an adjunct in chronically inflamed tissues.

Translational pediatrics
2025

Diagnostic value of prenatal ultrasound in the typing of fetal esophageal atresia.

Frontiers in medicine
2025

Thoracoscopic Posterior Tracheopexy After Esophageal Atresia Repair: A Case Report.

Asian journal of endoscopic surgery
2025

Esophageal magnetic compression anastomosis for esophageal atresia repair: when not to use magnets-our experience.

Surgical endoscopy
2025

Management of gastroesophageal reflux disease following esophageal atresia surgery: a systematic review.

Pediatric surgery international
2025

Mortality and Surgery-Related Complications in Very Low and Extreme Low Birth Weight Infants Treated for Esophageal Atresia: A Multi-Center Cohort Study.

Journal of pediatric surgery
2025

The Association of Environmental Exposure in the Etiology of Esophageal Atresia in Children: A Systematic Review and Meta-analysis.

Journal of pediatric surgery
2025

Acid suppression after esophageal atresia repair: Some infants do benefit.

Journal of pediatric gastroenterology and nutrition
2025

Delayed primary surgery and outcomes in children with gastrointestinal anomalies in 264 hospitals and 74 countries.

American journal of epidemiology
2025

Commentary on acid suppression after esophageal atresia repair-Some infants do benefit.

Journal of pediatric gastroenterology and nutrition
2025

Technical Skill Acquisition in Pediatric Minimally Invasive Surgery: Evaluation of a 3D-Printed Simulator for Thoracoscopic Esophageal Atresia Repair.

Healthcare (Basel, Switzerland)
2025

Technique for Consistent Selective Left Mainstem Intubation in Neonatal and Infantile Surgery.

The American surgeon
2025

Serial bronchoalveolar lavage as barium aspiration treatment. Case report.

Boletin medico del Hospital Infantil de Mexico
2025

Long-term outcomes after thoracoscopic versus open surgery for congenital esophageal atresia: propensity-score overlap weighting analysis.

Pediatric surgery international
2025

Balloon dilation therapy for managing anastomotic strictures subsequent to surgical correction of esophageal atresia.

Translational pediatrics
2025

Enhanced fetal MRI diagnosis of esophageal atresia using super-resolution slice-to-volume reconstruction.

Pediatric radiology
2025

Clinical outcomes of primary thoracoscopic repair in patients with esophageal atresia and tracheoesophageal fistula: A multicenter study from the East Asia pediatric surgery research consortium.

Journal of pediatric surgery
2025

The application of stay sutures in thoracoscopic esophageal repair for Type C esophageal atresia.

Pediatric surgery international
2025

Type C tracheoesophageal fistula, ventricular septal defect, and megacolon in a 37-week fetus - A case report.

International journal of surgery case reports
2025

Evaluation of mid- and long-term quality of life in patients operated on for esophageal atresia.

The Turkish journal of pediatrics
2025

The prevalence of iron deficiency in pediatric esophageal atresia.

Journal of pediatric gastroenterology and nutrition
2025

Systematic Review of the Prevalence of Gastrointestinal Congenital Anomalies: A Global and Regional Review Protocol.

Sage open pediatrics
2025

The Global Burden of Major Gastrointestinal Anomalies: A Global, Systematic Review of Gastrointestinal Anomaly Birth Prevalence.

Sage open pediatrics
2025

VACTERL association in a newborn as a product of a twin pregnancy by egg donation.

Cirugia y cirujanos
2025

Musculoskeletal Outcomes Following Thoracoscopic Versus Conventional Open Repair of Esophageal Atresia: A Systematic Review and Meta-Analysis from Pediatric Surgery Meta-Analysis (PESMA) Study Group.

Journal of pediatric surgery
2025

Thoracoscopic Salvage Surgery for Oesophageal Atresia is Feasible After Previous Thoracotomy.

Journal of pediatric surgery
2025

Esophageal atresia in three overseas departments compared with metropolitan France.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
2025

Predictive modeling for early detection of refractory esophageal stricture following esophageal atresia surgery: insight from a machine learning study.

Pediatric surgery international
2025

Mind the Missing Gap: A Cervical Variant of Type A Esophageal Atresia.

Children (Basel, Switzerland)
2025

Annular Pancreas: Insights Into the Diagnosis of a Rare Anatomical Malformation in Pediatric Patients.

Cureus
2025

Postoperative reintubation as risk factor for anastomotic stricture after congenital esophageal atresia.

Pediatric surgery international
2025

A Sudden Increase in Intrathoracic Pressure After Fibrin Glue Application During A Pediatric Thoracoscopic Surgery: A Case Report.

A&amp;A practice
2025

Diagnostic Challenges of Inherited Renal Tubular Dysgenesis.

American journal of medical genetics. Part A
2025

Multicentre Retrospective Analysis of Lung Function Impairment and Risks for Restrictive Syndrome During Childhood After Type III Esophageal Atresia Repair.

Journal of pediatric surgery
2025

Clinical challenges and outcomes of thoracoscopic versus open repair in esophageal atresia: a single-center retrospective comparative study.

Annals of surgical treatment and research
2025

Prevalence and risk factors of feeding difficulties in children with delayed reconstruction of esophageal atresia: a Swedish nationwide study.

Pediatric surgery international
2025

Clinical Utility of Indocyanine Green Fluorescence in Neonatal Surgery: A Single-Center Study and Systematic Review.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
2025

Laparoscopic "TOUSSEN" fundoplication for pediatric gastroesophageal reflux disease: a new modified technique gentle as Toupet and solid as Nissen?

Pediatric surgery international
2025

Post-intubation Tracheoesophageal Fistula Following Meningioma Excision: A Case Report and Literature Review.

Cureus
2025

Defining an Anastomotic Stricture Following Oesophageal Atresia Repair.

Journal of pediatric surgery
2025

Resource use in infants undergoing esophageal atresia repair at major children's hospitals.

Surgery
2025

Pressure controlled ventilation with volume guarantee improves outcomes in neonatal thoracoscopic esophageal atresia surgery.

Frontiers in pediatrics
2025

The boy who lived: staged repair of congenital diaphragmatic hernia with esophageal atresia and tracheoesophageal fistula in a 32-week, 1.5 kg infant, and review of the literature.

Journal of surgical case reports
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Maternal Systemic Lupus Erythematosus and Neonatal Outcomes: A Tertiary Single Center Hospital Experience in Turkey.

Fetal and pediatric pathology
2025

Long-Term Aerodigestive Morbidities After Esophageal Atresia/Tracheoesophageal Fistula Repair.

Journal of pediatric surgery
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Novel Mammillary Body Manual Segmentation: Application for Quantitative MRI Analysis of Critically Ill Infants.

Clinical neuroimaging (Hoboken, N.J.)
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Phenotypic Spectrum of KATNIP-Associated Joubert Syndrome: Possible Association with Esophageal Atresia and Review of the Literature.

Genes
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Disrupted endosomal trafficking of the Vangl-Celsr polarity complex underlies congenital anomalies in Xenopus trachea-esophageal morphogenesis.

Developmental cell
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Clinical insights from a rare case of neonatal upper gastrointestinal obstruction complicated by H-Type tracheoesophageal fistula: case report and review of the literature.

BMC pediatrics
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Long-gap esophageal atresia: a single center experience.

Frontiers in pediatrics
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COVID-19 Vaccination During Pregnancy and Birth Defects: Results From the CDC COVID-19 Vaccine Pregnancy Registry, United States 2021-2022.

Birth defects research
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Three cases of congenital diseases in the children of female semiconductor workers at a company recognized by the Occupational Disease Adjudication Committee.

Annals of occupational and environmental medicine
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Single-Stage Surgery for Persistent Cloaca With Vertebral Defects, Anal Atresia, Cardiac Defects, Tracheoesophageal Fistula or Atresia, Renal Anomalies, and Limb Defects (VACTERL) Association: A Case Report on Avoiding Temporary Colostomy.

Cureus
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Genetic Background of Eosinophilic Esophagitis and Esophageal Atresia in Children.

Digestive diseases and sciences
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Regenerative Response 35 Days After Esophageal Replacement in a Porcine Model; Technical Difficulties and Attempts to Achieve Optimal Tissue Remodeling.

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Outcomes of Virtually Assisted Personalized Tracheostomy Tubes for Congenital Airway Anomalies.

The Laryngoscope
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Impact of Muscle Paralysis After Primary Esophageal Atresia Repair.

Journal of pediatric surgery
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Longitudinal assessments of motor performance and musculoskeletal abnormalities in preschool children with esophageal atresia.

Early human development
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Exploring the intersection of caregiving burden, parenting stress, and self-efficacy in caregivers of children born with esophageal atresia.

Journal of pediatric nursing
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Thoracoscopic Stapling Ligation of H-Type Tracheo-Esophageal Fistula: A Viable and Safe Technique.

Journal of laparoendoscopic &amp; advanced surgical techniques. Part A
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Incidence of Recurrent Laryngeal Nerve Palsy in Thoracic Surgery in Neonates.

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Tips and Tricks in the Laparoscopic Treatment of Type I Duodenal Atresia: Description of a Technique.

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Esophageal Atresia and Tracheoesophageal Fistula: Diagnosis, Management, and Outcomes.

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Microcomputed Tomography in the Adriamycin Rat Model of Malformations-Preliminary Results.

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Posture and Physical Activity Levels of Parents of Children With Esophageal Atresia: A Comparative Study.

Child: care, health and development
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Rozhledy v chirurgii : mesicnik Ceskoslovenske chirurgicke spolecnosti
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Trio Exome Sequencing in VACTERL Association.

Kidney international reports
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Referências e fontes

Bases de dados externas citadas neste artigo

Publicações científicas

Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.

  1. Stricture classification of pediatric esophageal strictures (SCOPES): A novel tool to predict response to endoscopic therapy.
    Journal of pediatric gastroenterology and nutrition· 2026· PMID 41867120mais citado
  2. Neurodevelopmental assessment at 24 months in infants with esophageal atresia: A prospective cohort study.
    Journal of pediatric gastroenterology and nutrition· 2026· PMID 41854015mais citado
  3. Induced Pluripotent Stem Cells as a Tool to Decipher the Normal and Abnormal Development of the Esophagus and Trachea from Normal Morphogenesis to Esophageal Atresia, Tracheomalacia, and Laryngo-Tracheal Clefts.
    Cells· 2026· PMID 41827881mais citado
  4. Risk factors for anastomotic complications following thoracoscopic repair of type III esophageal atresia in neonates: a single-center retrospective cohort study.
    Frontiers in pediatrics· 2026· PMID 41782952mais citado
  5. Development of a lifelong core outcome set for oesophageal atresia &#xb1; tracheoesophageal fistula: the OCELOT study.
    BMJ open· 2026· PMID 41781041mais citado
  6. Trends and outcomes of thoracoscopic esophageal atresia and tracheoesophageal fistula repair: a retrospective analysis 2016-2022.
    Pediatr Surg Int· 2026· PMID 41984220recente
  7. Balancing two defects: surgical decision-making in low-birth-weight neonates with esophageal atresia and tetralogy of Fallot-a case series.
    BMC Pediatr· 2026· PMID 41965591recente
  8. Modified thoracoscopic anastomosis of esophageal atresia with tracheoesophageal fistula.
    Pediatr Surg Int· 2026· PMID 41964708recente
  9. Coloboma associated with VACTERL characterized by Ultra-Widefield Optical Coherence Tomography.
    Retin Cases Brief Rep· 2026· PMID 41961004recente
  10. Long-term Outcomes of Esophageal Replacement in Children: A Multicenter Study by the Indian Association of Pediatric Surgeons.
    J Indian Assoc Pediatr Surg· 2026· PMID 41958773recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:1199(Orphanet)
  2. OMIM OMIM:189960(OMIM)
  3. MONDO:0008586(MONDO)
  4. GARD:6381(GARD (NIH))
  5. Busca completa no PubMed(PubMed)
  6. Artigo Wikipedia(Wikipedia)
  7. Q298233(Wikidata)

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Atresia esofágica
Compêndio · Raras BR

Atresia esofágica

ORPHA:1199 · MONDO:0008586
Prevalência
1-5 / 10 000
Herança
Not applicable
CID-10
Q39.1 · Atresia de esôfago, com fístula traqueoesofágica
CID-11
Ensaios
11 ativos
Início
Neonatal
Prevalência
0.0 (Europe)
MedGen
UMLS
C0014850
EuropePMC
Wikidata
Wikipedia
Papers 10a
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