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Article

Transient leukoencephalopathy associated with X-linked Charcot-Marie-Tooth disease.

Journal of child neurology - 1 Aug 2010

Rosser Tena, Muir Jason, Panigrahy Ashok, Baldwin Erin E, Boles Richard G

Abstract excerpt

X-linked hereditary demyelinating neuropathy (Charcot-Marie-Tooth 1X) accounts for 10% to 20% of all hereditary demyelinating neuropathies and is caused by mutations in the GJB1 gene, which codes for connexin 32. Connexin 32 is a gap junction protein widely expressed in Schwann cells as well as oligodendrocytes. Transient leukoencephalopathy has been reported in children and adults with Charcot-Marie-Tooth 1X....

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Source

Identifiers

PMID: 20472869
DOI: 10.1177/0883073809352378

Genes

GJB1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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