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.
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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