Autosomal dominant adult-onset proximal spinal muscular atrophy

Disease Export to PDF
Name:
Autosomal dominant adult-onset proximal spinal muscular atrophy
Description:
A rare, genetic, motor neuron disease characterized by adulthood-onset of slowly progressive, proximal muscular weakness with fasciculations, amyotrophy, cramps, and absent/hypoactive reflexes, without bulbar or pyramidal involvement.
ORPHAcode:
209335
Synonyms:
Autosomal dominant adult-onset proximal SMA
Autosomal dominant late-onset spinal muscular atrophy, Finkel type
Finkel disease
SMAFK
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14