1.
J Indian Assoc Pediatr Surg
; 21(4): 193-195, 2016.
Article
in English
| MEDLINE
| ID: mdl-27695215
ABSTRACT
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 kidney that have not been reported in English literature.