DSpace@İnönü

Bardet-Biedl syndrome associated with vaginal atresia: a case report

Basit öğe kaydını göster

dc.contributor.author Uguralp, S
dc.contributor.author Demircan, M
dc.contributor.author Cetin, S
dc.contributor.author Sigirci, A
dc.date.accessioned 2022-03-16T11:18:53Z
dc.date.available 2022-03-16T11:18:53Z
dc.date.issued 2003
dc.identifier.uri http://hdl.handle.net/11616/56012
dc.description.abstract 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.
dc.source TURKISH JOURNAL OF PEDIATRICS
dc.title Bardet-Biedl syndrome associated with vaginal atresia: a case report


Bu öğenin dosyaları:

Dosyalar Boyut Biçim Göster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster