Raras
Buscar doenças, sintomas, genes...
Paralisia laríngea, congênita
ORPHA:137932CID-10 · J38.0CID-11 · LA71.YPCDT · SUSDOENÇA RARA
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Introdução

O que você precisa saber de cara

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Paralisia cerebral (PC) é um grupo de distúrbios de movimento que aparecem na primeira infância. Os sinais e sintomas variam entre as pessoas e ao longo do tempo, mas incluem má coordenação, músculos rígidos, músculos fracos e tremores. Pode haver problemas com sensação, visão, audição e fala. Frequentemente, bebês com paralisia cerebral não rolam, sentam, engatinham ou andam tão cedo quanto outras crianças. Outros sintomas podem incluir convulsões e problemas com o pensamento ou raciocínio. Embora os sintomas possam se tornar mais notáveis ao longo dos primeiros anos de vida, os problemas subjacentes não pioram com o tempo.

Publicações científicas
289 artigos
Último publicado: 2026 Jan
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SUS: Cobertura parcialScore: 50%
PCDT disponívelCentros em: PA, PE, BA, CE, PB +10CID-10: J38.0
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Sinais e sintomas

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

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico289PubMed
Últimos 10 anos109publicações
Pico201816 papers
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2026Hoje · 2026📈 2018Ano de pico🧪 2019Primeiro ensaio clínico
Publicações por ano (últimos 10 anos)

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Genética e causas

O que está alterado no DNA e como passa nas famílias

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Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

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Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

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Onde tratar no SUS

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

🇧🇷 Atendimento SUS — Paralisia laríngea, congênita

Centros de Referência SUS

24 centros habilitados pelo SUS para Paralisia laríngea, congênita

Centros para Paralisia laríngea, congênita

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.

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Publicações mais relevantes

Timeline de publicações
0 papers (10 anos)
#1

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

Journal of pediatric surgery2026 Feb

Vocal cord paralysis (VCP) and recurrent laryngeal nerve injury may be either congenital or acquired due to surgical trauma in patients with esophageal atresia and tracheoesophageal fistula (EA-TEF). A systematic review and meta-analysis were performed to define the risk factors for developing VCP and other nerve injuries. Systematic literature search was conducted for the period 2000 (Jan) to 2024 (Jan) under the PRISMA guidelines. The study protocol was registered on PROSPERO (CRD42024532277). EMBASE, MEDLINE and PUBMED databases were searched and qualitative and quantitative data were extracted relating to VCP, recurrent laryngeal and phrenic nerve injury in patients with EA-TEF. Statistical analysis was performed with CMA-V4 software. Among 1421 articles, 851 abstracts were screened for inclusion criteria. Full texts of 125 articles were assessed for eligibility. The subgroup analysis was performed in 8 articles for type of EA-TEF and 4 articles for type of surgery. The risk of VCP occurrence was increased 1.58 times in Type-A, 2.97 times in Type-B and 6.85 times in Type -E when compared to Type-C EA [95%CI: (0.95-2.63, p = 0.08), (0.96-9.17, p = 0.059), (3.23-14.52, p < 0,05), respectively]. There was no significant correlation between thoracotomy and thoracoscopy to risk of VCP occurrence [OR:1.85 (95 % CI 0.42-8.04), p = 0.41]. Kendal's Tau test and Egger's tests were performed revealing that there was no publication bias for all data. Although the risk of vocal cord paralysis was higher in other EA types compared to type C, a statistically significant difference was observed only between type C and type E. The surgical approach, whether thoracotomy or thoracoscopic, does not appear to be associated with the risk of vocal cord paralysis.

#2

Analysis of Factors Influencing Voice Outcome in Unilateral Vocal Fold Paresis and Paralysis.

World journal of otorhinolaryngology - head and neck surgery2025 Dec

To explore factors influencing voice outcome in patients with unilateral vocal fold paresis and paralysis (UVFP). A total of 578 patients diagnosed with UVFP by laryngeal electromyography and follow-up were included, including 286 males and 292 females, with an average age of (43.18 ± 14.65) years (13-80 years). According to follow-up analysis, the patients were divided into a vocal improvement group (VIG) and a vocal nonimprovement group (VNG), and the differences in etiology, nerve injury type (recurrent laryngeal nerve [RLN] alone or with superior laryngeal nerve [SLN] injury) and degree (incomplete or complete RLN injury) between the two groups were compared. There were 232 patients in the VIG and 346 patients in the VNG. In the VIG, 121 patients (52.16%) had idiopathic vocal fold paresis or paralysis, with a significantly higher proportion than the VNG (41.62%, p = 0.013). Patients with tumor compression, radiotherapy, or congenital factors only presented in the VNG, and there was no significant difference in the proportion of patients with different injury sites between the two groups. There was no significant difference in proportions of RLN injury and RLN+SLN injury between the two groups (p = 0.98). In the VIG, 168 patients (72.41%) had complete RLN injury, which was lower than the VNG (79.77%, p = 0.04). The specific injury types in thyroarytenoid muscles (TA) showed no differences between the two groups. But in posterior cricoarytenoid muscles (PCA) of the VIG, the proportion of decreased recruitment pattern combined with synkinesis was significantly reduced (p < 0.01). Idiopathic UVFP has a greater possibility of vocal improvement, while least possibilities were seen in those with tumor compression, radiotherapy, and congenital factors. Complete RLN injury is not conducive to vocal improvement, of which the PCA injury is more evident than TA muscle and PCA synkinesis may be a greater risk factor.

#3

A case report of tracheal duplication cyst with steatocystomatous histology: a rare embryological overlap.

BMC surgery2025 Nov 17

Tracheal duplication cysts (TDCs) are rare congenital anomalies caused by defects in the duplication of the foregut, that is of endodermal origin. These cysts are usually present during childhood and cases in adults are seen very rarely. Steatocystoma multiplex is a disorder of multiple sebaceous cysts, most commonly from skin appendages, that has ectodermal origin. The presence of the two coexisting in the same place has never been reported in literature. We report the first case of a unique embryological overlap between ectoderm and endoderm in a TDC. A 34-year-old Indian male presented with progressive hoarseness and a change in voice. Laryngoscopy revealed left vocal cord paralysis. MRI of the neck done later showed a 3 cm cystic mass in the left tracheoesophageal groove, which was compressing the left recurrent laryngeal nerve. It was surgically excised, and the histopathology revealed a cyst lined by cuboidal epithelium with numerous sebaceous gland nests consistent with steatocystoma multiplex. These findings confirmed a tracheal duplication cyst with unique ectodermal differentiation in this patient. Our case stands out for its first-of-its-kind embryological overlap and also for its surgical management. The lack of respiratory epithelium and the presence of sebaceous glands (ectodermal) within a TDC (endodermal) suggest a misdirected embryologic development of the foregut. Dermoid, teratoma, branchial cleft cysts, laryngeal cysts, and malignancy were ruled out. Even though these cysts are benign, they may cause airway obstruction, vocal cord palsy, or other associated compressive symptoms. The treatment of choice for these cysts is en bloc removal, because incomplete excision has been reported to have increased recurrence. Although malignant transformation is rare, histopathological examination is required to rule it out. This is the first reported case of a tracheal duplication cyst with steatocystoma-like histology. It identified the need to consider rare embryologic overlaps while evaluating neck cysts and highlights the importance of thorough histopathological examination for better diagnosis and management.

#4

Diagnostic accuracy of laryngeal ultrasound in the evaluation of stridor at a tertiary care pediatric center in India.

International journal of pediatric otorhinolaryngology2025 Nov

Pediatric airway assessment with endoscopy puts forth certain challenges. Laryngeal Ultrasound (LUS) is a non-invasive imaging modality that enables evaluation of laryngeal dynamics. This study aims to assess the clinical utility and diagnostic accuracy of LUS in diagnosing pediatric stridor by comparing its findings with endoscopic assessment. This prospective blinded cohort study included patients aged between 0 and 17 years, presenting with stridor. Those previously diagnosed were excluded. All patients were subjected to a Laryngeal Ultrasound followed by a Microlaryngoscopy and Bronchoscopy (MLB). Sensitivity, specificity, and positive and negative predictive values for LUS were calculated compared to the gold standard. We describe 26 patients with stridor, with a median age of 4 months. LUS was able to correctly identify 21/26 cases (80.76 %), with the most common cause being laryngomalacia in 11/26 cases (42.3 %). Other pathologies identified were subglottic stenosis, vocal fold palsies, vallecular cysts, and glottic masses (papilloma). The overall diagnostic accuracy of laryngeal ultrasound in identifying the cause of pediatric stridor was calculated and sensitivity was found to be 78.26 % (95 % CI: 56.3-92.54 %), specificity 100 % (95 % CI: 29.24-100 %), positive predictive value 100 % (95 % CI: 81.47-100 %) and negative predictive value 37.5 % (95 % CI: 21.65-56.58 %). Laryngeal Ultrasound can increasingly be used as a first-line, non-invasive airway assessment tool that can be repeated at the bedside for screening purposes. Our study found a high specificity and positive predictive value for Laryngeal Ultrasound in diagnosing Pediatric stridor. Its routine use to assess the pediatric larynx could potentially help in the selection of stridulous children for MLB.

#5

Unilateral Vocal Cord Paralysis Caused by Cervical Esophageal Duplication Cyst Containing a Foreign Body: A Case Report.

Surgical case reports2025

Cervical esophageal duplication is a rare congenital anomaly that occasionally causes compressive symptoms. Herein, we present a unique case of unilateral vocal cord paralysis caused by a cervical esophageal duplication cyst with a granuloma containing a foreign body. A 10-year-old boy presented with a 1.5-month history of hoarseness and choking. Laryngoscopy revealed left vocal cord paralysis, and CT revealed a mass near the inferior pole of the left thyroid lobe. Fine-needle aspiration cytology revealed no evidence of malignancy. Ultrasonography and MRI findings suggested an esophageal duplication cyst with an inflammatory granuloma. Antibiotic therapy was ineffective, and a surgical approach was considered. The esophageal duplication cyst was resected through a collar incision, and a film-like foreign body with granulation tissue was extracted from the abscess. The recurrent laryngeal nerve was preserved, and the vocal cord function improved within 2 months. This case highlights the unusual presentation of an inflamed cervical esophageal duplication cyst with an embedded foreign body, which resulted in recurrent laryngeal nerve impairment and subsequent unilateral vocal cord paralysis. Early surgical intervention with careful nerve preservation can result in a functional recovery.

Publicações recentes

Ver todas no PubMed

📚 EuropePMCmostrando 109

2025

Analysis of Factors Influencing Voice Outcome in Unilateral Vocal Fold Paresis and Paralysis.

World journal of otorhinolaryngology - head and neck surgery
2025

A case report of tracheal duplication cyst with steatocystomatous histology: a rare embryological overlap.

BMC 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

Diagnostic accuracy of laryngeal ultrasound in the evaluation of stridor at a tertiary care pediatric center in India.

International journal of pediatric otorhinolaryngology
2025

Unilateral Vocal Cord Paralysis Caused by Cervical Esophageal Duplication Cyst Containing a Foreign Body: A Case Report.

Surgical case reports
2025

Is there a role for whole genome sequencing in idiopathic vocal fold immobility?

International journal of pediatric otorhinolaryngology
2025

Bilateral vocal fold paralysis after cardiac surgery managed with anterior-posterior cricoid split.

The Journal of laryngology and otology
2025

Outcomes of laryngeal surgery in children with congenital laryngomalacia and neurological and neurodevelopmental comorbidities - A NSQIP analysis.

International journal of pediatric otorhinolaryngology
2025

Endoscopic Anteroposterior Cricoid Split in Idiopathic Bilateral Vocal Fold Immobility in Newborns: A Consecutive Case Series.

The Laryngoscope
2025

Is Outpatient Supraglottoplasty Possible? Examination of Perioperative Comorbidities and Outcomes.

Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
2024

Surgical Treatments of Pediatric Bilateral Vocal Fold Paralysis: A Systematic Review.

Journal of otolaryngology - head &amp; neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale
2025

Neurophysiological Assessment in Children with Vocal Fold Paralysis: A Tertiary Center Experience.

The Laryngoscope
2024

Ortner's syndrome due to aneurysmal dilatation of the left pulmonary artery secondary to mixed pulmonary valve disease.

BMJ case reports
2024

The anatomic repair of recurrent aortic arch obstruction in children and adolescents.

JTCVS open
2024

Management of Pediatric Bilateral Vocal Fold Paralysis: A State-of-the-Art Review of Etiologies, Diagnosis, and Treatments.

Children (Basel, Switzerland)
2024

Strategies for CO2 Laser Use in Laryngeal Microsurgery: A Systematic Review.

Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
2024

Laryngeal Structural Dysphagia in Children.

Otolaryngologic clinics of North America
2023

Giving Voice to Cardiovocal Syndrome: A 26-Year-Old Woman With Hypophonia and Dysphagia.

Cureus
2024

Clinical Prognosis of Vocal Cord Paralysis After Cardiothoracic Surgery in Infants.

Pediatric cardiology
2024

Vocal Cord Paralysis after Repair of Esophageal Atresia.

European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie
2023

A case report of the rare non recurrent laryngeal nerve in a resource limited setting: The first Ethiopian documentation.

International journal of surgery case reports
2024

Ultrasound Screening After Cardiac Surgery Shows Vocal Fold Impairment and Predicts Aspiration.

The Laryngoscope
2023

Unilateral sublingual nerve paralysis after laryngeal mask airway in a patient with congenital heart disease: a case report.

The Journal of international medical research
2022

A Unique Cause of Upper Airway Obstruction in a Child: Laryngeal Lipoma.

Turkish archives of otorhinolaryngology
2023

Neonatal stridor presents at home - vocal fold paralysis as rare presenting feature of CHARGE syndrome.

Case reports in perinatal medicine
2023

Safety and effectiveness of vocal fold injection laryngoplasty in infants less than one year of age.

International journal of pediatric otorhinolaryngology
2023

[Clinical application of modified fistulectomy in the treatment of congenital pyriform sinus fistula based on segmental anatomy of fistula].

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery
2024

Kommerell's diverticulum: an unusual cause of unilateral vocal cord palsy?

Annals of the Royal College of Surgeons of England
2022

A safe and effective surgical method for complex pyriform sinus fistula.

Laryngoscope investigative otolaryngology
2022

The clinical application of flexible bronchoscopy in a neonatal intensive care unit.

Frontiers in pediatrics
2022

Genome Wide Association Study with Imputed Whole Genome Sequence Data Identifies a 431 kb Risk Haplotype on CFA18 for Congenital Laryngeal Paralysis in Alaskan Sled Dogs.

Genes
2022

Stridor caused by duplication cyst in a female infant and temporary vocal cord paralysis. A case report.

International journal of surgery case reports
2022

Laryngeal electromyography, a useful tool in difficult cases of pediatric laryngeal mobility disorders.

International journal of pediatric otorhinolaryngology
2022

Ortner's Syndrome in an Infant With Congenital Heart Disease.

Journal of medical cases
2022

Suture lateralization in congenital bilateral vocal cord immobility in neonates and infants: A hybrid approach.

International journal of pediatric otorhinolaryngology
2022

Laryngeal pathologies in dysphonic children with Down Syndrome.

International journal of pediatric otorhinolaryngology
2022

The changing face of paediatric airway endoscopic surgery: An 8-year single surgeon review.

International journal of pediatric otorhinolaryngology
2022

The incidence of recurrent laryngeal nerve injury resulting in vocal cord paralysis following interventional congenital catheterisation procedures.

Cardiology in the young
2022

Xq27.1 palindrome mediated interchromosomal insertion likely causes familial congenital bilateral laryngeal abductor paralysis (Plott syndrome).

Journal of human genetics
2023

Open paediatric laryngotracheal reconstruction: a five-year experience at a tertiary referral centre.

The Journal of laryngology and otology
2023

[Upper Airway Obstruction in a Type 4 Laryngeal Palmar in Infant].

Le Mali medical
2021

[Innovative surgical solutions for laryngeal stenoses in newborns and infants].

Orvosi hetilap
2022

Evaluating dysphagia in infants with congenital heart disease using Fiberoptic Endoscopic Evaluation of Swallowing.

International journal of pediatric otorhinolaryngology
2022

Slide Tracheoplasty for Repair of Complex Tracheoesophageal Fistulas.

The Laryngoscope
2021

Incidence and Recovery of Vocal Fold Immobility Following Pediatric Cardiac Operations.

World journal for pediatric &amp; congenital heart surgery
2021

The utility of handheld ultrasound as a point-of-care screening tool to assess vocal fold impairment following congenital heart surgery.

International journal of pediatric otorhinolaryngology
2023

Efficiency and Safety of Patent Ductus Arteriosus Surgical Ligation in Extremely Low Birth Weight Infants Without Chest Tube Placement.

Journal of pediatric intensive care
2021

Congenital airway anomalies.

Seminars in pediatric surgery
2021

Third branchial cleft cyst as a cause of hoarseness: a case report.

The Journal of international medical research
2021

Carotid Endarterectomy for a Patient with a Right-sided Aortic Arch and Aberrant Left Subclavian Artery Predicting a Left Non-recurrent Inferior Laryngeal Nerve: A Case Report and Literature Review.

NMC case report journal
2022

Clinical and Financial Outcomes Associated With Vocal Fold Paralysis in Congenital Cardiac Surgery.

Journal of cardiothoracic and vascular anesthesia
2021

Diagnostic and management strategies for congenital H-type tracheoesophageal fistula: a systematic review.

Pediatric surgery international
2021

Factors associated to functional recovery of left vocal fold motion impairment at two-years-old age in very preterm infants.

International journal of pediatric otorhinolaryngology
2020

A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy.

Genes
2021

Cardiovascular Hoarseness (Ortner's Syndrome): A Pictorial Review.

Current problems in diagnostic radiology
2020

Ortner's Syndrome as a Presenting Feature of Congenital Heart Disease in Infants.

Heart views : the official journal of the Gulf Heart Association
2021

Surgical Management of Bilateral Vocal Fold Paralysis in Children: A Systematic Review and Meta-analysis.

Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
2020

The usefulness of intraoperative neurological monitoring for esophageal cancer with double aortic arch; a case report.

BMC surgery
2020

[Congenital laryngeal paralysis in children].

Vestnik otorinolaringologii
2020

Bilateral Selective Laryngeal Reinnervation for Bilateral Vocal Fold Paralysis in Children.

JAMA otolaryngology-- head &amp; neck surgery
2019

Endoscopic Preoperative Assessment, Classification of Stenosis, Decision-Making.

Frontiers in pediatrics
2019

Left recurrent laryngeal nerve palsy following aortic arch stenting: A case report.

World journal of cardiology
2020

Esophagectomy for Esophageal Cancer in a Patient with Left Pulmonary Artery Sling.

Annals of surgical oncology
2019

Kommerell's diverticulum: rare cause of unilateral vocal cord palsy.

BMJ case reports
2020

Orofacial motor dysfunction in Moebius syndrome.

Developmental medicine and child neurology
2019

Current Epidemiology of Vocal Cord Dysfunction After Congenital Heart Surgery in Young Infants.

Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
2020

Prognosis of congenital idiopathic abductor laryngeal paralysis with laryngeal electromyography.

The Laryngoscope
2019

Surgical and therapeutic advances in the management of voice problems in children and young people.

Current opinion in otolaryngology &amp; head and neck surgery
2019

Repair of type IV laryngotracheoesophageal cleft (LTEC) on ECMO.

Pediatric surgery international
2019

Endoscopic arytenoid abduction lateropexy for the treatment of neonatal bilateral vocal cord paralysis - Long-term results.

International journal of pediatric otorhinolaryngology
2019

Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene.

International journal of pediatric otorhinolaryngology
2018

[Clinical evaluation of vocal fold paralysis in 207 children].

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
2019

Medialization Laryngoplasty in Pediatric Patients With Unilateral Vocal Fold Immobility: A Case Series.

The Annals of otology, rhinology, and laryngology
2018

Employing bioabsorbable grafts in two-stage laryngotracheal reconstruction of pediatric patient with severe subglottic stenosis and history of airway surgery.

International journal of pediatric otorhinolaryngology
2018

Common causes of congenital stridor in infants.

JAAPA : official journal of the American Academy of Physician Assistants
2018

Congenital laryngeal paralysis in Alaskan Huskies: 25 cases (2009-2014).

Journal of the American Veterinary Medical Association
2018

Revealing the needs of children with tracheostomies.

European annals of otorhinolaryngology, head and neck diseases
2018

[Phoniatric outcomes of endoscopic arytenoid abduction lateropexy in patients with transient bilateral vocal cord paralysis].

Orvosi hetilap
2018

Airway evaluation in children with single ventricle cardiac physiology.

International journal of pediatric otorhinolaryngology
2018

Familial impairment of vocal cord mobility in childhood with clubfoot.

Clinical dysmorphology
2018

Pediatric Asthma Masqueraders.

The journal of allergy and clinical immunology. In practice
2018

Congenital and iatrogenic laryngeal and vocal abnormalities in patients with 22q11.2 deletion.

International journal of pediatric otorhinolaryngology
2018

Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study.

Lancet (London, England)
2018

Analysis of Vocal Fold Motion Impairment in Neonates Undergoing Congenital Heart Surgery.

JAMA otolaryngology-- head &amp; neck surgery
2018

Risk Factors for Gastrostomy Tube Placement in Single Ventricle Patients Following The Norwood Procedure.

Seminars in thoracic and cardiovascular surgery
2018

Cervicothoracoscopic Approach for Esophageal Cancer in a Patient with Right-Sided Aortic Arch.

Annals of surgical oncology
2018

Branchial anomalies in children: A report of 105 surgical cases.

International journal of pediatric otorhinolaryngology
2018

Silent aspiration: Who is at risk?

The Laryngoscope
2017

Neonatal Stridor in Familial Congenital Laryngeal Paralysis (Plott Syndrome): 
A Case Study in an Omani Family.

Oman medical journal
2017

Vocal Fold Immobility due to Birth Trauma: A Systematic Review and Pooled Analysis.

Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
2017

Recurrent Laryngeal Nerve Injury and Swallowing Dysfunction in Neonatal Aortic Arch Repair.

The Annals of thoracic surgery
2017

A novel variation of the recurrent laryngeal nerve.

BMC surgery
2017

New trends in rehabilitation of children with ENT disorders.

Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale
2017

Congenital H-type tracheoesophageal fistula: A multicenter review of outcomes in a rare disease.

Journal of pediatric surgery
2016

Aetiological profile of paediatric stridor in a Malaysian tertiary hospital.

Malaysian family physician : the official journal of the Academy of Family Physicians of Malaysia
2017

Transoral robotic surgery for the pediatric head and neck surgeries.

European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
2016

Laryngomalacia: Our Clinical Experience.

Turkish archives of otorhinolaryngology
2017

Tracheostomy Among Infants With Hypoplastic Left Heart Syndrome Undergoing Cardiac Operations: A Multicenter Analysis.

The Annals of thoracic surgery
2017

A new solution for neonatal bilateral vocal cord paralysis: Endoscopic arytenoid abduction lateropexy.

The Laryngoscope
2017

Laryngeal ultrasound and vocal fold movement in the pediatric cardiovascular intensive care unit.

The Laryngoscope
2016

Congenital H-type tracheoesophageal fistula: a national multicenter study.

Pediatric surgery international
2016

Outcomes of recurrent laryngeal nerve injury following congenital heart surgery: A contemporary experience.

Journal of the Saudi Heart Association
2016

Microtrapdoor Flap Technique for Treatment of Glottic Laryngeal Stenosis: Experience With 34 Cases.

Journal of voice : official journal of the Voice Foundation
2015

Surgical and nonsurgical management of patent ductus arteriosus in cats: 28 cases (1991-2012).

Journal of the American Veterinary Medical Association
2015

Managing dysphonia in paediatric patients with complex airway conditions.

The Journal of laryngology and otology
2015

JS-X syndrome: A multiple congenital malformation with vocal cord paralysis, ear deformity, hearing loss, shoulder musculature underdevelopment, and X-linked recessive inheritance.

International journal of pediatric otorhinolaryngology
2015

Ductus arteriosus aneurysm and vocal cord paralysis.

Circulation
2015

Familial congenital bilateral vocal fold paralysis: a novel gene translocation.

International journal of pediatric otorhinolaryngology
2015

Spontaneous recovery of bilateral congenital idiopathic laryngeal paralysis: systematic non-meta-analytical review.

International journal of pediatric otorhinolaryngology

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Comunidades

Grupos ativos de quem convive com esta doença aqui no Raras

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Doenças relacionadas

Doenças com sintomas parecidos — ajudam quem ainda está buscando diagnóstico

Ainda não achamos doenças com sintomas parecidos o suficiente.

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. Nerve injury and vocal cord paralysis after esophageal atresia and tracheoesophageal fistula repair: Systematic review and meta-analysis.
    Journal of pediatric surgery· 2026· PMID 41242420mais citado
  2. Analysis of Factors Influencing Voice Outcome in Unilateral Vocal Fold Paresis and Paralysis.
    World journal of otorhinolaryngology - head and neck surgery· 2025· PMID 41477133mais citado
  3. A case report of tracheal duplication cyst with steatocystomatous histology: a rare embryological overlap.
    BMC surgery· 2025· PMID 41250047mais citado
  4. Diagnostic accuracy of laryngeal ultrasound in the evaluation of stridor at a tertiary care pediatric center in India.
    International journal of pediatric otorhinolaryngology· 2025· PMID 41092657mais citado
  5. Unilateral Vocal Cord Paralysis Caused by Cervical Esophageal Duplication Cyst Containing a Foreign Body: A Case Report.
    Surgical case reports· 2025· PMID 41058884mais citado
  6. Cries, Stridor, and Clues: Unmasking a Rare Airway Obstruction in an Infant.
    Cureus· 2026· PMID 41717171recente
  7. ASXL3 gene variants causing Bainbridge-Ropers syndrome: clinical and genetic analysis of four Chinese patients.
    Front Neurosci· 2025· PMID 41659201recente
  8. 3D-printed EXOs/BMSCs composite hydrogel scaffolds for thyroid cartilage defect repair.
    Biomed Mater· 2026· PMID 41554255recente
  9. [Clinical and genetic characteristics of X-linked intellectual disability associated with HUWE1 gene variants].
    Zhonghua Er Ke Za Zhi· 2025· PMID 41233135recente
  10. Management of congenital laryngeal webs in young children: a clinical study of 22 cases.
    Eur Arch Otorhinolaryngol· 2025· PMID 41094216recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:137932(Orphanet)
  2. MONDO:0015316(MONDO)
  3. Esclerose Lateral Amiotrofica(PCDT · Ministério da Saúde)
  4. GARD:12713(GARD (NIH))
  5. Busca completa no PubMed(PubMed)
  6. Q55785389(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

Compêndio · Raras BR

Paralisia laríngea, congênita

ORPHA:137932 · MONDO:0015316
🇧🇷 Brasil SUS
Geral
CID-10
J38.0 · Paralisia das cordas vocais e da laringe
CID-11
Início
Neonatal
MedGen
UMLS
C0396058
Wikidata
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