SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY: Difference between revisions
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'''OVERVIEW''' | |||
A [[scapuloperoneal spinal muscular atrophy]] is a rare [[autosomal dominant]] genetic motor neuron disease characterized by predominantly motor axonal peripheral neuropathy manifesting with progressive scapuloperoneal spinal muscular atrophy and weakness, laryngeal palsy, congenital absence of muscles, and, in some, skeletal abnormalities. | |||
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Revision as of 20:47, 17 April 2024
OVERVIEW
A scapuloperoneal spinal muscular atrophy is a rare autosomal dominant genetic motor neuron disease characterized by predominantly motor axonal peripheral neuropathy manifesting with progressive scapuloperoneal spinal muscular atrophy and weakness, laryngeal palsy, congenital absence of muscles, and, in some, skeletal abnormalities.