A Turner syndrome case associated with anal atresia, interrupted aortic arch and multicystic dysplastic kidney
TURKISH JOURNAL OF PEDIATRICS, cilt.52, sa.2, ss.215-217, 2010 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 52 Sayı: 2
- Basım Tarihi: 2010
- Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.215-217
- Karadeniz Teknik Üniversitesi Adresli: Evet
Özet
Mutlu M, Dilber E, Asian Y, Okten A, ozturk O. A Turner syndrome case associated with anal atresia, interrupted aortic arch and multicystic dysplastic kidney. Turk J Pediatr 2010; 52: 215-217. Although renal and cardiac malformations are commonly seen in Turner syndrome (TS), anorectal malformations, multicystic dysplastic kidney and interrupted aortic arch are quite rare in TS. A newborn with TS with three quite rare congenital malformations (imperforate anus/anal atresia associated with rectovestibular fistula, interrupted aortic arch, and multicystic dysplastic kidney) is presented.