Raras
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Atresia do cólon
ORPHA:1198CID-10 · Q42.9CID-11 · LB16.0OMIM 303650DOENÇA RARA

A atresia colônica é uma malformação intestinal congênita que resulta em um segmento não latente do cólon e caracterizada por obstrução intestinal inferior que se manifesta com distensão abdominal e falha na passagem de mecônio em recém-nascidos.

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Introdução

O que você precisa saber de cara

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A atresia colônica é uma malformação intestinal congênita que resulta em um segmento não latente do cólon e caracterizada por obstrução intestinal inferior que se manifesta com distensão abdominal e falha na passagem de mecônio em recém-nascidos.

Publicações científicas
193 artigos
Último publicado: 2026 Feb

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
Unknown
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
0.0
Worldwide
Início
Antenatal
+ neonatal
🏥
SUS: Cobertura mínimaScore: 35%
Centros em: PA, PE, BA, CE, PB +10CID-10: Q42.9
🇧🇷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
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Entender a doença

Do básico ao detalhe, leia no seu ritmo

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Sinais e sintomas

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

Características mais comuns

90%prev.
Úlcera péptica
Muito frequente (99-80%)
90%prev.
Atresia colônica
Muito frequente (99-80%)
55%prev.
Anormalidade da morfologia do mesentério
Frequente (79-30%)
55%prev.
Estenose duodenal
Frequente (79-30%)
17%prev.
Gastrosquise
Ocasional (29-5%)
17%prev.
Onfalocele
Ocasional (29-5%)
8sintomas
Muito frequente (2)
Frequente (2)
Ocasional (4)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 8 características clínicas mais associadas, ordenadas por frequência.

Úlcera pépticaPeptic ulcer
Muito frequente (99-80%)90%
Atresia colônicaColonic atresia
Muito frequente (99-80%)90%
Anormalidade da morfologia do mesentérioAbnormality of mesentery morphology
Frequente (79-30%)55%
Estenose duodenalDuodenal stenosis
Frequente (79-30%)55%
GastrosquiseGastroschisis
Ocasional (29-5%)17%

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico193PubMed
Últimos 10 anos62publicações
Pico202310 papers
Linha do tempo
2026Hoje · 2026🧪 2010Primeiro ensaio clínico📈 2023Ano 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-clínico5
Medicamentos catalogadosEnsaios clínicos· 0 medicamentos · 5 ensaios
Carregando informações de tratamento...

Onde tratar no SUS

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

🇧🇷 Atendimento SUS — Atresia do cólon

Centros de Referência SUS

24 centros habilitados pelo SUS para Atresia do cólon

Centros para Atresia do cólon

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

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Publicações mais relevantes

Timeline de publicações
60 papers (10 anos)
#1

Successful Surgery for Type III Colonic Atresia Using the Side-to-Side Santulli Procedure: Rescue Treatment During the Practice of Global Pediatric Surgery.

Cureus2026 Feb

Colonic atresia (CA) is a rare congenital intestinal condition that requires surgical intervention. The surgical approaches for its treatment may vary from primary anastomosis to stoma creation. We report a case of CA treated with side-to-side anastomosis and Santulli-type colostomy. A three-year-old girl with a history of CA who had undergone ascending colostomy in the neonatal period visited the surgical mission of the World Surgical Foundation for definitive surgical management. The details of the operative findings in the neonatal period are unknown. Preoperative contrast enema revealed an unused rectosigmoid segment, suggesting that primary end-to-end anastomosis would be challenging. Exploratory laparotomy revealed type III CA in the ascending colon. The distal colon, from the transverse to the descending colon, was absent. Due to the 5-fold caliber difference between the ascending and sigmoid colon, a side-to-side Santulli procedure with an end colostomy was performed to restore colonic continuity. The procedure effectively restored intestinal continuity and addressed a significant caliber discrepancy. Postoperative recovery was uneventful, with consistent colostomy output and normal rectal stool defecation. Two months postoperatively, the patient remained in a good general condition and had a favorable bowel function. In conclusion, the side-to-side Santulli procedure offers a safe approach for CA, providing an additional safeguard as a pressure-release valve for cases with significant caliber differences between the proximal and distal colon, ensuring smooth stool passage.

#2

Intestinal Atresia in Finland: Maternal Risk Factors, Prevalence, Associated Anomalies and Survival.

Acta paediatrica (Oslo, Norway : 1992)2026 Jan 14

We aimed to investigate prevalence, associated anomalies and survival of congenital intestinal atresia and to examine maternal risk factors for jejunoileal atresia (JIA). All children born with, or pregnancies terminated because of, JIA or colonic atresia (CA) in Finland during 1987-2019 were identified from the Finnish Register of Congenital Malformations. Clinical information was obtained from national health registers. Maternal risk factors were assessed using all JIA cases from 2004 to 2017 (n = 101). For each case, five appropriately matched live-born controls were selected. We identified 175 JIA and 48 CA cases. About half were isolated anomalies. Gastrointestinal anomalies were the most common associated defects (26% in JIA, 35% in CA), followed by cardiac anomalies in JIA (13%) and urinary tract anomalies in CA (19%). Survival was 88% in JIA and 94% in CA. Only two of 224 patients died directly due to intestinal atresia. Maternal insulin use (adjusted odds ratio [aOR] 8.4, 95% CI 1.4-51.0) and propionic acid derivatives (aOR 4.6, 95% CI 1.5-14.8) were associated with increased JIA risk. Although associated anomalies were frequent, mortality in intestinal atresia remained low. Maternal insulin and propionic acid derivative use may meaningfully contribute to JIA risk. IV.

#3

Colonic web in infants and toddlers: a cause of chronic bowel obstruction.

BMJ case reports2025 Jul 13

Colonic web, a rare subtype of colonic atresia, typically presents in the neonatal period. However, delayed presentation, as seen in our cases, poses significant diagnostic and therapeutic challenges. We report two cases-an infant and a toddler-who presented with chronic constipation, abdominal distension and failure to thrive. Both patients were stabilised and underwent exploratory laparotomy, which confirmed the diagnosis of colonic web. A surgery involving web excision and diversion colostomy was performed successfully. Postoperative recovery was uneventful, and both patients demonstrated significant improvement during follow-up. These cases highlight the importance of maintaining a broad differential diagnosis in older infants and toddlers with obstructive bowel symptoms, the utility of imaging and intraoperative findings for diagnosis and the need for careful follow-up to rule out coexisting conditions like Hirschsprung Disease.

#4

Balloon dilatation therapy for postoperative bowel stricture following primary anastomosis of colonic atresia: A case report.

Pediatrics and neonatology2025 May
#5

Prevalence, risk factors and mortality associated with colonic atresia: a population-based case-control study.

Pediatric surgery international2025 Dec 23

This study aims to explore maternal and pregnancy-related risk factors for colonic atresia (CA) and assess the national total prevalence, mortality, and frequency of co-occurring anomalies of this rare malformation in 2004-2017. This case-control study involved 36 cases with congenital CA identified from several Finnish registers. All cases were identified based on the ICD-9/ICD-10 codes and classified based on co-occurring anomalies. Five controls without gastrointestinal congenital malformations matched for residence and time of conception (± 1 year) were randomly selected for each case. Maternal risk factors were analyzed with data from the same registers. Total prevalence of CA was 0.45/10,000, birth prevalence was 0.37/10,000 and live birth prevalence was 0.36/10,000. The overall prevalence trend did not change (p = 0.11) during the study period. There were 15 (41.7%) isolated cases, 3 (8.3%) were associated with known syndromes and 18 (50.0%) had multiple congenital anomalies. Together there were 19.4% (n = 7) terminations or neonatal mortalities. An association was observed with maternal diabetes and CA (p = 0.03). The prevalence of CA in Finland is low with no significant change over the study period. Despite the high frequency of associated anomalies, the overall survival of CA is very high, 97%.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC105 artigos no totalmostrando 62

2026

Successful Surgery for Type III Colonic Atresia Using the Side-to-Side Santulli Procedure: Rescue Treatment During the Practice of Global Pediatric Surgery.

Cureus
2026

Intestinal Atresia in Finland: Maternal Risk Factors, Prevalence, Associated Anomalies and Survival.

Acta paediatrica (Oslo, Norway : 1992)
2025

Prevalence, risk factors and mortality associated with colonic atresia: a population-based case-control study.

Pediatric surgery international
2025

A neonate with meconium peritonitis, first-trimester hepatitis A affected pregnancy: A case report.

SAGE open medical case reports
2025

Distal Ileal Atresia in a Preterm Infant with Minor Omphalocele: A Case Report.

Surgical case reports
2025

Colonic web in infants and toddlers: a cause of chronic bowel obstruction.

BMJ case reports
2025

Factors influencing early surgical outcomes of intestinal atresia in a resource-limited tertiary center.

Pediatric surgery international
2025

A Rare Case of Apple Peel Ileal Atresia With Coexisting Colonic Atresia: Surgical Management and Outcomes.

Cureus
2025

Transverse colonic atresia with rectal atresia in a neonate - A rare case of double-site intestinal atresia.

International journal of surgery case reports
2025

Balloon dilatation therapy for postoperative bowel stricture following primary anastomosis of colonic atresia: A case report.

Pediatrics and neonatology
2024

Progressive colonic stenosis in an infant: Successful treatment with endoscopic balloon dilation.

JPGN reports
2025

Decisions in Diversion: Enterostomy vs. Primary Anastomosis for Colonic Atresia.

Journal of pediatric surgery
2024

Colonic atresia and Hirschsprung's disease in a neonate: A case report.

International journal of surgery case reports
2024

Acquired colonic atresia in children: a report of three cases and review of the literature.

Journal of surgical case reports
2024

Management and Outcomes of Intestinal Atresia - A Single Institution Experience From 1947 to 2019.

Journal of pediatric surgery
2024

Minimally Invasive Placement of Pedicle Screws Using Robotic-Assisted Navigation and Magnetically Controlled Growing Rods in a Patient with Early-Onset Scoliosis: Technical Note and Case Report.

Journal of orthopaedic case reports
2024

CLINICAL FEATURES OF THE COURSE OF HIRSCHSPRING'S DISEASE INCHILDREN OF THE FIRST YEAR.

Georgian medical news
2024

Sigmoid atresia: Case report and literature review.

International journal of surgery case reports
2023

Congenital Segmental Dilatation of Ascending Colon with Distal Microcolon: A Diagnostic Dilemma.

Journal of Indian Association of Pediatric Surgeons
2023

Type III colonic atresia in a 6-week-old kitten.

JFMS open reports
2023

Colonic Atresia Associated with Biliary Atresia.

Journal of Indian Association of Pediatric Surgeons
2023

Imaging Features of Neonatal Bowel Obstruction.

Radiographics : a review publication of the Radiological Society of North America, Inc
2023

Distal colonic atresia: a case report.

Journal of surgical case reports
2023

Colonic atresia and hirschsprung disease: a case report and review of the literature.

Journal of medical case reports
2023

Windsock or Cobra Head Sign: A Distinctive Imaging Sign to Differentiate Type 1 Colonic Atresia From Hirschsprung's Disease.

Cureus
2022

Factors associated with mortality in congenital malformations of the gastrointestinal tract in a tertiary center in Senegal.

World journal of pediatric surgery
2022

Midgut Atresia: Diagnostic and Management Challenges From Northern Tanzania.

Clinical medicine insights. Pediatrics
2022

Intestinal atresia and necrotizing enterocolitis: Embryology and anatomy.

Seminars in pediatric surgery
2022

[Delayed meconium passage due to malrotation and colon atresia].

Nederlands tijdschrift voor geneeskunde
2022

Large Colon Volvulus in a Neonatal Foal Secondary to Atresia Coli.

Journal of equine veterinary science
2023

Differences in the Outcome of Colonic Atresia with and without Abdominal Wall Defects.

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

Pre-pregnancy exposure to arsenic in diet and non-cardiac birth defects.

Public health nutrition
2022

The colonic diaphragm in an infant.

Asian journal of surgery
2022

Acquired Colonic Atresia in a Six-Week-Old Infant.

Indian journal of pediatrics
2023

Gastroschisis Complicated by Colonic Atresia.

The American surgeon
2021

Staged Repair Using Modified Bishop-Koop Procedure in Complicated Congenital Colonic Atresia in a Neonate.

Cureus
2021

Anorectal malformation, associated with colon atresia and intestinal malrotation, a case report.

International journal of surgery case reports
2021

Colonic atresia: a rare entity in the newborn. A six-case report and a bibliographic review.

Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica
2021

Diagnostic decision-making tool for imaging term neonatal bowel obstruction.

Clinical radiology
2020

Diagnostic performance and role of the contrast enema for low intestinal obstruction in neonates.

Pediatric surgery international
2020

Congenital multiple colonic atresias with intestinal malrotation: a case report.

Surgical case reports
2020

Challenges and Outcome of Management of Gastroschisis at a Tertiary Institution in North-Eastern Nigeria.

Frontiers in surgery
2019

Early diagnosis and surgical intervention untie the Gordian knot in newborns with colonic atresia: report of two cases and review of the literature.

Folia medica Cracoviensia
2019

Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.

Birth defects research
2018

Demographic Study and Management of Colonic Atresia: Single-Center Experience with Review of Literature.

Journal of Indian Association of Pediatric Surgeons
2018

Maternal genitourinary infections and risk of birth defects in the National Birth Defects Prevention Study.

Birth defects research
2018

Radiological feature of colonic atresia.

Archives of disease in childhood. Fetal and neonatal edition
2017

Population-based birth defects data in the United States, 2010-2014: A focus on gastrointestinal defects.

Birth defects research
2018

Maternal report of fever from cold or flu during early pregnancy and the risk for noncardiac birth defects, National Birth Defects Prevention Study, 1997-2011.

Birth defects research
2017

Disparity in access and outcomes for emergency neonatal surgery: intestinal atresia in Kampala, Uganda.

Pediatric surgery international
2016

Intestinal Atresia: Experience at a Busy Center of North-West India.

Journal of neonatal surgery
2016

Congenital Neonatal Intestinal Obstruction: Retrospective Analysis at Tertiary Care Hospital.

Journal of neonatal surgery
2016

Colonic Atresia: Association with Other Anomalies.

Journal of neonatal surgery
2016

Alimentary Tract Atresias associated with Anorectal Malformations: 10 Years' Experience.

Journal of neonatal surgery
2016

Gallbladder Duplication Associated with Gastro-Intestinal Atresia.

Journal of neonatal surgery
2016

Multiple Congenital Colonic Stenosis: A Rare Gastrointestinal Malformation.

Case reports in pediatrics
2017

Role of intraluminal bowel echogenicity on prenatal ultrasounds to determine the anatomical level of intestinal atresia.

The journal of maternal-fetal &amp; neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
2015

The Combination of Gastroschisis, Jejunal Atresia, and Colonic Atresia in a Newborn.

Case reports in pediatrics
2015

Colonic atresia associated with annular pancreas: An extremely rare and previously unreported association.

Journal of Indian Association of Pediatric Surgeons
2014

Colonic Atresia due to Internal Herniation through the Falciform Ligament Defect: A Case Report.

Journal of neonatal surgery
2015

Atresia of the Colon Associated with Hirschsprung's Disease.

Archives of Iranian medicine
2015

Maternal occupational exposure to ionizing radiation and major structural birth defects.

Birth defects research. Part A, Clinical and molecular teratology
Ver todos os 105 no EuropePMC

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Doenças relacionadas

Doenças com sintomas parecidos — ajudam quem ainda está buscando diagnóstico

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. Successful Surgery for Type III Colonic Atresia Using the Side-to-Side Santulli Procedure: Rescue Treatment During the Practice of Global Pediatric Surgery.
    Cureus· 2026· PMID 41798460mais citado
  2. Intestinal Atresia in Finland: Maternal Risk Factors, Prevalence, Associated Anomalies and Survival.
    Acta paediatrica (Oslo, Norway : 1992)· 2026· PMID 41532961mais citado
  3. Colonic web in infants and toddlers: a cause of chronic bowel obstruction.
    BMJ case reports· 2025· PMID 40659383mais citado
  4. Balloon dilatation therapy for postoperative bowel stricture following primary anastomosis of colonic atresia: A case report.
    Pediatrics and neonatology· 2025· PMID 40118768mais citado
  5. Prevalence, risk factors and mortality associated with colonic atresia: a population-based case-control study.
    Pediatric surgery international· 2025· PMID 41432778mais citado
  6. A neonate with meconium peritonitis, first-trimester hepatitis A affected pregnancy: A case report.
    SAGE Open Med Case Rep· 2025· PMID 40717837recente
  7. Distal Ileal Atresia in a Preterm Infant with Minor Omphalocele: A Case Report.
    Surg Case Rep· 2025· PMID 40678017recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:1198(Orphanet)
  2. OMIM OMIM:303650(OMIM)
  3. MONDO:0010562(MONDO)
  4. GARD:1446(GARD (NIH))
  5. Busca completa no PubMed(PubMed)
  6. Q55782541(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 do cólon
Compêndio · Raras BR

Atresia do cólon

ORPHA:1198 · MONDO:0010562
Prevalência
Unknown
Herança
Not applicable
CID-10
Q42.9 · Ausência, atresia e estenose congênita de partes não especificadas do cólon (intestino grosso)
CID-11
Início
Antenatal, Neonatal
Prevalência
0.0 (Worldwide)
MedGen
UMLS
C0266190
EuropePMC
Wikidata
Papers 10a
DiscussaoAtiva

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