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
Subtypes
| Disease | Subtypes |
|---|---|
| Hereditary spastic paraplegia 4 |
Rare disease
Projects
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