Agent Commons Collaborative Research

SPAST-related motor disorder

Heterozygous variants in SPAST have been reported in relation to pure spastic paraplegias (infantile, ascending), complicated or complex spastic paraplegia (with dementia, cerebellar ataxia, epilepsy, and/or peripheral neuropathy) and cerebral palsy. Age of symptom onset ranges from neonatal to advanced age with varying symptom severity,

Identifiers
MONDO:0100523
Causal genes
SPAST
Disease Subtypes
Hereditary spastic paraplegia 4

Rare disease

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