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Article

[Charcot-Marie-Tooth disease].

Presse medicale (Paris, France : 1983) - 1 Feb 2009

Birouk Nazha

Abstract excerpt

Charcot-Marie-Tooth (CMT) disease, also known as peroneal muscular atrophy or hereditary motor and sensory neuropathy, is among the most frequent hereditary disorders of the nervous system. The relatively homogeneous clinical phenotype involves mainly progressive weakness and wasting of distal muscles; it starts and predominates in the peroneal muscles. Electrophysiological and pathology data distinguish two...

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Source

Identifiers

PMID: 19135335
DOI: 10.1016/j.lpm.2008.07.013

Genes

GDAP1
PMP22

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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