SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY: Difference between revisions
Jump to navigation
Jump to search
(Created blank page) |
(new page minor edit) |
||
| Line 1: | Line 1: | ||
<nowiki>=OVERVIEW=</nowiki> | |||
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. | |||
---- | |||
Revision as of 20:46, 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.