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- Title
Coexisting urogenital anomaly and duodenal atresia in two atypical Holt--Oram syndrome.
- Authors
Ahmet Ali, Tuncer; Afra, Karavelioğlu; Embleton Didem, Baskin; Muhsin, Elmas
- 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.
- Subjects
KIDNEY abnormalities; DUODENUM abnormalities; MULTIPLE human abnormalities; ATRIAL septal defects; CONGENITAL heart disease; GENITOURINARY organ abnormalities; ARM abnormalities; GENETICS; DIAGNOSIS
- Publication
Journal of Indian Association of Pediatric Surgeons, 2016, Vol 21, Issue 4, p193
- ISSN
0971-9261
- Publication type
Article
- DOI
10.4103/0971-9261.186552