SPAST-related motor disorder

MONDO:0100523

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,

2 clinical trials for this condition and its sub-types, 0 tagged with SPAST-related motor disorder itself.

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↑ Central nervous system disorder (20397) ↑ Hereditary neurological disease (5772)

Sub-types of SPAST-related motor disorder

Hereditary spastic paraplegia 4 2 trials

Including sub-types (2) Tagged with SPAST-related motor disorder (0)

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