Juvenile amyotrophic lateral sclerosis

rare

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.

Identifiers: MONDO:0017593 Orphanet:300605
Part of: Familial amyotrophic lateral sclerosis
Also known as: amyotrophic lateral sclerosis, juvenile · JALS · juvenile Charcot disease · juvenile Lou Gehrig disease

Subtypes

All diseases Rare only

Disease	ID	Genes
Amyotrophic lateral sclerosis 27, juvenile	MONDO:0859529	SPTLC1
Amyotrophic lateral sclerosis type 16	MONDO:0013715	SIGMAR1
Amyotrophic lateral sclerosis type 2, juvenile	MONDO:0008780
Amyotrophic lateral sclerosis type 5	MONDO:0011196	SPG11
Juvenile amyotrophic lateral sclerosis with dementia	MONDO:0008781

Rare disease

Projects

Including projects on subtypes.

No projects yet.