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PedAM

Pediatric Disease Annotations & Medicines




Disease muscular atrophy
Phenotype C0442874|neuropathy
Sentences 1
PubMedID- 21252112 Charcot-marie-tooth disease type 1a is a hypertrophic de-remyelinating neuropathy manifesting with peroneal muscular atrophy and uniform, marked, slowing of nerve conduction velocities.

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