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Article

Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?

Brain and behavior - 1 Apr 2016

Werheid Friederike, Azzedine Hamid, Zwerenz Eva, Bozkurt Ahmet, Moeller Marcus J, Lin Lilian, Mull Michael, Häusler Martin, Schulz Jörg B, Weis Joachim, Claeys Kristl G

Abstract excerpt

INTRODUCTION: Charcot-Marie-Tooth neuropathy (CMT) is a genetically heterogeneous group of peripheral neuropathies. In addition to the classical clinical phenotype, additional features can occur. METHODS: We studied a wide range of additional features in a cohort of 49 genetically confirmed CMT patients and performed a systematic literature revision. RESULTS: Patients harbored a PMP22 gene alteration (n = 28) or...

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Source

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Identifiers

PMID: 27088055
DOI: 10.1002/brb3.451
PMCID: PMC4782242

Genes

MPZ
LITAF
MFN2
PMP22
GJB1
INF2
NEFL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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