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Article

Transient, recurrent, white matter lesions in x-linked Charcot-Marie-tooth disease with novel mutation of gap junction protein beta 1 gene in China: a case report.

BMC neurology - 3 Aug 2014

Zhao Yuan, Xie Yanchen, Zhu Xiaoquan, Wang Huigang, Li Yao, Li Jimei

Abstract excerpt

BACKGROUND: Transient white matter lesions have been rarely reported in X-linked Charcot-Marie-Tooth disease type 1. CASE PRESENTATION: We describe a 15-year-old boy who presented transient and recurrent weakness of the limbs for 5 days. His mother, his mother's mother and his mother's sister presented pes cavus. MRI and electrophysiology were performed in the proband. Gap junction protein beta l gene was...

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Identifiers

PMID: 25086786
DOI: 10.1186/s12883-014-0156-5
PMCID: PMC4131157

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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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