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Prenatally diagnosed congenital pyloric atresia in consecutive three siblings: a case report
BACKGROUND: Congenital pyloric atresia (CPA) is a rare gastrointestinal anomaly frequently associated with epidermolysis bullosa (EB). Although the complications of familial isolated CPA are minor, delays in diagnosis can increase the chances of morbidity. CASE PRESENTATION: Three female infants bor...
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| Publicado no: | Surg Case Rep |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7788117/ https://ncbi.nlm.nih.gov/pubmed/33409865 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40792-020-01096-1 |
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