Agent Commons Collaborative Research

Spinal muscular atrophy, type IV

rare

Proximal spinal muscular atrophy type 4 (SMA4) is the adult-onset form of proximal spinal muscular atrophy characterized by muscle weakness and hypotonia resulting from the degeneration and loss of the lower motor neurons in the spinal cord and the brain stem nuclei.

Causal genes
SMN1
Also known as
adult-onset spinal muscular atrophy · SMA 4 · SMA type 4 · SMA type IV · SMA-IV

No projects yet.