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Neurology. 1998 May;50(5):1477-80.

Congenital muscular dystrophy and cerebellar atrophy.

Author information

  • 1Department of Neuropediatrics, Höpital St. Eloi, Montpellier, France.

Abstract

Two siblings and two other unrelated patients had congenital muscular weakness and dystrophic changes but normal immunocytochemical stainings for merosin, dystrophin, and dystrophin-related proteins on muscle biopsy. All had marked ataxia and cerebellar atrophy or hypoplasia. Cerebral white matter and cortical organization appeared normal.

PMID:
9596013
[PubMed - indexed for MEDLINE]
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