| CASE REPORT |
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| 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
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0971-9261.186552
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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