Journal of Indian Association of Pediatric Surgeons
Journal of Indian Association of Pediatric Surgeons
                                                   Official journal of the Indian Association of Pediatric Surgeons                           
Year : 2016  |  Volume : 21  |  Issue : 4  |  Page : 193--195

Coexisting urogenital anomaly and duodenal atresia in two atypical Holt-Oram syndrome


Tuncer Ahmet Ali1, Karavelioglu Afra2, Baskin Embleton Didem2, Elmas Muhsin3 
1 Department of Paediatric Surgery, Yuksekova State Hospital, Hakkari, Turkey
2 Department of Paediatric Surgery, Afyon Kocatepe University, Afyonkarahisar, Turkey
3 Department of Medical Genetic, Faculty of Medicine, Afyon Kocatepe University, Afyonkarahisar, Turkey

Correspondence Address:
Tuncer Ahmet Ali
Department of Paediatric Surgery, Yuksekova State Hospital, Hakkari 30300
Turkey

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.


How to cite this article:
Ali TA, Afra K, Didem BE, Muhsin E. Coexisting urogenital anomaly and duodenal atresia in two atypical Holt-Oram syndrome.J Indian Assoc Pediatr Surg 2016;21:193-195


How to cite this URL:
Ali TA, Afra K, Didem BE, Muhsin E. Coexisting urogenital anomaly and duodenal atresia in two atypical Holt-Oram syndrome. J Indian Assoc Pediatr Surg [serial online] 2016 [cited 2021 Jan 25 ];21:193-195
Available from: https://www.jiaps.com/article.asp?issn=0971-9261;year=2016;volume=21;issue=4;spage=193;epage=195;aulast=Ali;type=0