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.
Comprehensive, easy-to-understand information about this condition
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amyotrophic lateral sclerosis type 1
MONDO:0007103
frontotemporal dementia and/or amyotrophic lateral sclerosis 1
MONDO:0007105
spinocerebellar ataxia type 2
MONDO:0008458
amyotrophic lateral sclerosis type 2, juvenile
MONDO:0008780
juvenile amyotrophic lateral sclerosis with dementia
MONDO:0008781
amyotrophic lateral sclerosis type 15
MONDO:0010459