Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Spinal muscular atrophy · Neuronopathy, distal hereditary motor, autosomal recessive
Neuronopathy, distal hereditary motor, autosomal recessive 3
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.
This condition has no sub-types.