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Neu-Laxova syndrome: a case report.

Abstract
Neu-Laxova syndrome is a rare congenital disorder characterized by microcephaly, limb contactures, lissencephaly and ichthyosis. A case of Neu-Laxova syndrome is presented, with a discussion of clinical manifestations, complications, and therapeutic interventions.
AuthorsPatrick Hickey, Elizabeth Piantanida, Sarah Lentz-Kapua, Julie Kenner
JournalPediatric dermatology (Pediatr Dermatol) Vol. 20 Issue 1 Pg. 25-7 ( 2003) ISSN: 0736-8046 [Print] United States
PMID12558841 (Publication Type: Case Reports, Journal Article)
Topics
  • Abnormalities, Multiple (diagnosis, therapy)
  • Brain (abnormalities)
  • Disease Progression
  • Fatal Outcome
  • Humans
  • Ichthyosis (complications, diagnosis)
  • Infant, Newborn
  • Limb Deformities, Congenital (complications, diagnosis)
  • Male
  • Microcephaly (complications, diagnosis)
  • Rare Diseases
  • Risk Assessment
  • Syndrome

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