Muscular Atrophy, Spinal


Adult Onset Spinal Muscular Atrophy

Adult Spinal Muscular Atrophy

Adult-Onset Spinal Muscular Atrophy

Amyotrophies, Spinal

Amyotrophy, Neurogenic Scapuloperoneal, New England Type

Amyotrophy, Spinal

Atrophies, Progressive Muscular

Atrophy, Myelopathic Muscular

Atrophy, Progressive Muscular

Atrophy, Spinal Muscular

Bulbospinal Neuronopathies

Bulbospinal Neuronopathy

Distal Spinal Muscular Atrophy

Hereditary Motor Neuronopathies

Hereditary Motor Neuronopathy

Motor Neuronopathies, Hereditary

Motor Neuronopathy, Hereditary

Muscular Atrophies, Progressive

Muscular Atrophy, Adult Spinal

Muscular Atrophy, Myelopathic

Muscular Atrophy, Progressive

Myelopathic Muscular Atrophy

Myelopathic Muscular Atrophy, Progressive

Neuronopathies, Bulbospinal

Neuronopathies, Hereditary Motor

Neuronopathy, Bulbospinal

Neuronopathy, Hereditary Motor

Oculopharyngeal Spinal Muscular Atrophy

Progressive Muscular Atrophies

Progressive Muscular Atrophy

Progressive Myelopathic Muscular Atrophy

Progressive Proximal Myelopathic Muscular Atrophy

Proximal Myelopathic Muscular Atrophy, Progressive

Scapuloperoneal Form of Spinal Muscular Atrophy

Scapuloperoneal Spinal Muscular Atrophy

Spinal Amyotrophies

Spinal Amyotrophy

Spinal Muscular Atrophy

Spinal Muscular Atrophy, Distal

Spinal Muscular Atrophy, Oculopharyngeal

Spinal Muscular Atrophy, Scapuloperoneal

Spinal Muscular Atrophy, Scapuloperoneal Form

A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)