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Complete familial Currarino triad in association with Hirschsprung's disease: magnetic resonance imaging features and the spectrum of anorectal malformations.

Abstract
Currarino syndrome, a rare hereditary condition, is defined as a partial sacral agenesis associated with a presacral mass and anorectal malformation. The authors present two siblings with complete Currarino triad and their mother with incomplete triad. The complete Currarino triad in the older sibling was associated with Hirschsprung's disease as the second reported case in the literature. Anorectal malformations, whether suspected of Currarino syndrome or not, should be examined with lumbosacral magnetic resonance imaging.
AuthorsO Kilickesmez, I Hakki Gol, M Uzun, C Oruk
JournalActa radiologica (Stockholm, Sweden : 1987) (Acta Radiol) Vol. 47 Issue 4 Pg. 422-6 (May 2006) ISSN: 0284-1851 [Print] Sweden
PMID16739705 (Publication Type: Case Reports, Journal Article)
Topics
  • Abnormalities, Multiple (diagnosis, surgery)
  • Anal Canal (abnormalities, pathology, surgery)
  • Child
  • Child, Preschool
  • Female
  • Hirschsprung Disease (complications)
  • Humans
  • Lipoma (diagnosis, surgery)
  • Magnetic Resonance Imaging
  • Male
  • Rare Diseases
  • Rectum (abnormalities, pathology, surgery)
  • Sacrum (abnormalities, pathology)
  • Spinal Neoplasms (diagnosis, surgery)

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