A Turner syndrome case associated with anal atresia, interrupted aortic arch and multicystic dysplastic kidney

MUTLU M., DİLBER E., ASIAN Y., Okten A. N., OZTURK O.

TURKISH JOURNAL OF PEDIATRICS, cilt.52, sa.2, ss.215-217, 2010 (SCI-Expanded) identifier identifier identifier

  • 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.