A carregar...
Coexisting urogenital anomaly and duodenal atresia in two atypical Holt–Oram syndrome
Holt–Oram syndrome (HOS) is a rare autosomal dominant disorder, characterized by upper limb dysplasia and congenital cardiac defect. We report two cases with HOS, first associated with renal agenesis, coronal hypospadias, urethral duplication and second associated with duodenal atresia and horseshoe...
Na minha lista:
| Publicado no: | J Indian Assoc Pediatr Surg |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4980884/ https://ncbi.nlm.nih.gov/pubmed/27695215 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-9261.186552 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|