Juvenile amyotrophic lateral sclerosis

MONDO:0017593

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.

Also known as: JALS, juvenile Charcot disease, juvenile Lou Gehrig disease, amyotrophic lateral sclerosis, juvenile

10 clinical trials for this condition and its sub-types, 0 tagged with Juvenile amyotrophic lateral sclerosis itself.

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Part of

↑ Familial amyotrophic lateral sclerosis (29)

Sub-types of Juvenile amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis type 16 0 trials
Amyotrophic lateral sclerosis type 2, juvenile 0 trials
Amyotrophic lateral sclerosis type 5 0 trials
Juvenile amyotrophic lateral sclerosis with dementia 0 trials

Including sub-types (10) Tagged with Juvenile amyotrophic lateral sclerosis (0)

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