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 İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 52 Konu: 2
  • Basım Tarihi: 2010
  • Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
  • Sayfa Sayıları: ss.215-217

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.