Dejerine-Sottas syndrome

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Dejerine-Sottas syndrome

ORPHA:64748Disease

Also called Charcot-Marie-Tooth disease type 3 · HMSN 3 · HMSN III · Hereditary motor and sensory neuropathy type 3 · Hereditary motor and sensory neuropathy type III

What it is

A clinical entity that represents a severe phenotype of Charcot-Marie-Tooth disease characterized by onset occurring in infancy, severe motor weakness, delayed motor development, extremely slow nerve conduction (PMP22 (17p12), MPZ (1q22), EGR2 (10q21.1) and PRX (19q13.2) have been implicated.

Key facts

Prevalence
<1 / 1 000 000
Age of onset
Infancy
Inheritance
Autosomal dominant, Autosomal recessive, Not applicable
Classified as
Disease

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Genes

EGR2Disease-causing germline mutation(s)
MPZDisease-causing germline mutation(s)
PMP22Disease-causing germline mutation(s)
PRXDisease-causing germline mutation(s) (loss of function)

ICD-10 codes

G60.0filed under a broader ICD-10 category — shared with 94 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 9204MONDO 0007790OMIM 145900OMIM 618184UMLS C0011195

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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