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

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


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
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0971-9261.186552

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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.






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  2005 - Journal of Indian Association of Pediatric Surgeons | Published by Wolters Kluwer - Medknow 

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