Bardet Biedl syndrome associated with vaginal atresia a case report
| dc.authorid | 7768 | en_US |
| dc.contributor.author | Uğuralp, Sema | |
| dc.contributor.author | Demircan, Mehmet | |
| dc.contributor.author | Çetin, Selma | |
| dc.contributor.author | Sığırcı, Ahmet | |
| dc.date.accessioned | 2017-06-24T07:16:07Z | |
| dc.date.available | 2017-06-24T07:16:07Z | |
| dc.date.issued | 2003 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description.abstract | Uğuralp S, Demircan M, Çetin S, Sığırcı A. Bardet-Biedl syndrome associated with vaginal atresia: a case report. Turk J Pediatr 2003; 45: 273- 275. This is a case report of Bardet-Biedl syndrome associated with vaginal atresia diagnosed in a 15-year-old girl. She had mild mental retardation; obesity; nistagmus, retinitis pigmentosa and optic atrophy in both eyes; accessory digit on the left hand; polydactyly in lower extremities; a mobile, painful, nonfixed mass of 6 cm in diameter in the pelvic region; a palpable cystic mass in front of the rectal wall; and no vaginal opening. Secondary sex characteristics were determined. The vaginal atresia was distinguished from vaginal agenesis by the presence of proximal vagina in radiological examination. | en_US |
| dc.identifier.citation | Uğuralp, S. Demircan, M. Çetin, S. Sığırcı, A. (2003). Bardet Biedl syndrome associated with vaginal atresia a case report. Turk J Pediatr. ; 45; 273-275 . | en_US |
| dc.identifier.endpage | 275 | en_US |
| dc.identifier.startpage | 273 | en_US |
| dc.identifier.uri | https://hdl.handle.net/11616/7176 | |
| dc.identifier.volume | 45 | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Turk J Pediatr | en_US |
| dc.relation.ispartof | Turk J Pediatr | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Bardet-Biedl syndrome | en_US |
| dc.subject | Vaginal atresia | en_US |
| dc.title | Bardet Biedl syndrome associated with vaginal atresia a case report | en_US |
| dc.type | Article | en_US |
