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Congenital muscular dystrophy x200

Last updated on Monday, March 23 2009 by gliageek

Congenital muscular dystrophy x200

This section came from the thigh of a 6-year-old boy with a family history of muscle weakness. Although routine neuro- imaging was normal, autopsy demonstrated subtle neuronal migration defects with focal cobblestone lissencephaly, consistent with Fukayama muscular dystrophy.

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