Juvenile amyotrophic lateral sclerosis

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Name:
Juvenile amyotrophic lateral sclerosis
Description:
Juvenile amyotrophic lateral sclerosis (JALS) is a very rare severe motor neuron disease characterized by progressive upper and lower motor neuron degeneration causing facial spasticity, dysarthria, and gait disorders with onset before 25 years of age.
ORPHAcode:
300605
Synonyms:
JALS
Juvenile Charcot disease
Juvenile Lou Gehrig disease
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14