Distal hereditary motor neuropathy type 2

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Name:
Distal hereditary motor neuropathy type 2
Description:
A rare autosomal dominant distal hereditary motor neuropathy characterized by onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life. Sensory involvement is typically less pronounced or absent. The severity of the condition is variable, and both lower and upper extremities may be involved.
ORPHAcode:
139525
Synonyms:
Distal spinal muscular atrophy type 2
dHMN2
dSMA2
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14