Distal hereditary motor neuropathy type 1

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Distal hereditary motor neuropathy type 1

Synonyms: Autosomal dominant distal juvenile spinal muscular atrophy type 1 | dHMN1

Distal hereditary motor neuropathy type 1 is a rare neuromuscular disease characterized by slowly-progressive lower limb muscular weakness and atrophy without sensory impairment. Additional clinical features may include pes cavus hammertoe and increased muscle tone.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024

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Distal hereditary motor neuropathy type 1?

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