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Pontocerebellar hypoplasia with microcephaly and dyskinesia: report of two cases.

Abstract
We present two clinically diagnosed cases of pontocerebellar hypoplasia with microcephaly and dyskinesia (pontocerebellar hypoplasia type 2) from two different Portuguese families. Both children presented neurological involvement from birth, progressive microcephaly, exuberant chorea and dystonia, myoclonic jerks, pontocerebellar hypoplasia, and progressive cerebral cortical atrophy. One child had consanguineous parents.
AuthorsC Barbot, G Carneiro, J Melo
JournalDevelopmental medicine and child neurology (Dev Med Child Neurol) Vol. 39 Issue 8 Pg. 554-7 (Aug 1997) ISSN: 0012-1622 [Print] England
PMID9295852 (Publication Type: Case Reports, Journal Article)
Topics
  • Atrophy
  • Cerebellopontine Angle (abnormalities, pathology)
  • Cerebral Cortex (pathology)
  • Child
  • Chorea (complications)
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Microcephaly (complications)
  • Movement Disorders (complications)

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