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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ali, Tuncer Ahmet, Afra, Karavelioğlu, Didem, Baskin Embleton, Muhsin, Elmas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980884/
https://www.ncbi.nlm.nih.gov/pubmed/27695215
http://dx.doi.org/10.4103/0971-9261.186552

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980884/
https://www.ncbi.nlm.nih.gov/pubmed/27695215
http://dx.doi.org/10.4103/0971-9261.186552

Ejemplares similares