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MURCS association with encephalocele: report of a second case.

Abstract
We report a female fetus with occipital encephalocele, dysraphism of the cervical spine, right renal agenesis and Mullerian agenesis. Additional findings included posterior cleft palate, absent left umbilical artery and Meckel's diverticulum. This fetus had the features of MURCS association with occipital encephalocele. This is the second report of encephalocele with MURCS association.
AuthorsM Suri, L A Brueton, N Venkatraman, P M Cox
JournalClinical dysmorphology (Clin Dysmorphol) Vol. 9 Issue 1 Pg. 31-3 (Jan 2000) ISSN: 0962-8827 [Print] England
PMID10649794 (Publication Type: Case Reports, Journal Article, Review)
Topics
  • Abnormalities, Multiple (pathology)
  • Cervical Vertebrae (abnormalities)
  • Cleft Palate (pathology)
  • Encephalocele (pathology)
  • Female
  • Humans
  • Infant, Newborn
  • Kidney (abnormalities)
  • Meckel Diverticulum (pathology)
  • Mullerian Ducts (abnormalities)
  • Umbilical Arteries (abnormalities)

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