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.
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Authors | C Barbot, G Carneiro, J Melo |
Journal | Developmental medicine and child neurology
(Dev Med Child Neurol)
Vol. 39
Issue 8
Pg. 554-7
(Aug 1997)
ISSN: 0012-1622 [Print] England |
PMID | 9295852
(Publication Type: Case Reports, Journal Article)
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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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