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Article

Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.

Muscle & nerve - 1 Nov 2002

Plante-Bordeneuve Violaine, Said Gérard

Abstract excerpt

Dejerine-Sottas disease (DSD) was originally described as a hypertrophic polyneuropathy characterized by onset in infancy or early childhood in patients born to unaffected parents. The clinical features included distal sensory changes with ataxia; pes cavus, at times with kyphoscoliosis; motor deficit and atrophy predominating in the distal lower limbs and progressing toward the proximal limbs following a...

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Source

Identifiers

PMID: 12402282
DOI: 10.1002/mus.10197

Genes

EGR2
PMP22

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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