A childhood spinal muscular atrophy that is evident before birth and characterized by diminished movement in the womb, joint deformities, extremely weak muscle tone and very weak respiratory muscles.
Comprehensive, easy-to-understand information about this condition
Checking for content...
No external resources available.
spinal muscular atrophy-progressive myoclonic epilepsy syndrome
MONDO:0008045
scapuloperoneal spinal muscular atrophy, autosomal dominant
MONDO:0008408
spinal muscular atrophy, facioscapulohumeral type
MONDO:0008452
adult-onset proximal spinal muscular atrophy, autosomal dominant
MONDO:0008453
spinal muscular atrophy, segmental
MONDO:0008455
spinal muscular atrophy, Ryukyuan type
MONDO:0010057