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, vol.52, no.2, pp.215-217, 2010 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 52 Issue: 2
  • Publication Date: 2010
  • Journal Name: TURKISH JOURNAL OF PEDIATRICS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.215-217
  • Karadeniz Technical University Affiliated: Yes

Abstract

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.