Scapuloperoneal spinal muscular atrophy

Disease Export to PDF
Name:
Scapuloperoneal spinal muscular atrophy
Description:
A rare, genetic motor neuron disease characterized by predominantly motor axonal peripheral neuropathy manifesting with progressive scapuloperoneal muscular atrophy and weakness, laryngeal palsy, congenital absence of muscles, and, in some, skeletal abnormalities.
ORPHAcode:
431255
Synonyms:
Neurogenic scapuloperoneal amyotrophy, New England type
SPSMA
Scapuloperoneal neuronopathy
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14