Distal spinal muscular atrophy type 3

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Synonyms: Autosomal recessive distal spinal muscular atrophy type 3 | Distal hereditary motor neuropathy type 3 and type 4 | dHMN3 and dHMN4 | dSMA3

Distal spinal muscular atrophy type 3 is a rare neuromuscular disease characterized by progressive muscular weakness and atrophy predominantly affecting distal parts of limbs later involvement of proximal and trunk muscles with marked hyperlordosis and late diaphragmatic dysfunction.

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 June 2024

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Distal spinal muscular atrophy type 3?

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