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A rare form of intestinal atresia characterized by the presence of numerous atresic segments in the small bowel (duodenum) or large bowel and leading to symptoms of intestinal obstruction: vomiting, abdominal bloating and inability to pass meconium in newborns.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for multiple intestinal atresia.
6 publications have been identified in PubMed for multiple intestinal atresia. Research spans Case Report / Case Series (60%) and Review / Meta-Analysis (40%).
Imhoff J (2025). [PMID: 40685546](https://pubmed.ncbi.nlm.nih.gov/40685546/). *Am J Med Genet A*. [Review / Meta-Analysis]
Al Rawahi Y (2025). [PMID: 40324929](https://pubmed.ncbi.nlm.nih.gov/40324929/). *BMJ Case Rep*. [Case Report / Case Series]
Badawi MA (2025). [PMID: 39444084](https://pubmed.ncbi.nlm.nih.gov/39444084/). *Pediatr Dev Pathol*. [Case Report / Case Series]
Huang Z (2025). [PMID: 39873864](https://pubmed.ncbi.nlm.nih.gov/39873864/). *Clin Rev Allergy Immunol*. [Review / Meta-Analysis]
Pérez Ramírez J (2024). [PMID: 39760601](https://pubmed.ncbi.nlm.nih.gov/39760601/). *Andes Pediatr*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 3:38 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center