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Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome.

Abstract
Five children are described with a striking, asymmetric facial appearance, craniosynostosis, preaxial polysyndactyly, agenesis of the corpus callosum and unusual skin with streaky areas of atrophy. The gut and mucous membranes are involved in two patients. This paper includes two patients described by Gorlin (1990) under the designation of the Curry Jones syndrome.
AuthorsI K Temple, D M Eccles, R M Winter, M Baraitser, S B Carr, D Shortland, M C Jones, C Curry
JournalClinical dysmorphology (Clin Dysmorphol) Vol. 4 Issue 2 Pg. 116-29 (Apr 1995) ISSN: 0962-8827 [Print] England
PMID7606318 (Publication Type: Case Reports, Journal Article)
Topics
  • Abnormalities, Multiple (physiopathology)
  • Agenesis of Corpus Callosum
  • Corpus Callosum (growth & development)
  • Face (abnormalities)
  • Female
  • Humans
  • Infant, Newborn
  • Intestines (abnormalities)
  • Male
  • Skin (growth & development)
  • Skin Abnormalities
  • Skull (abnormalities)
  • Syndactyly
  • Syndrome

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