Hereditary spastic paraplegia type 73 (SPG73)
Evidence-based neurology checklist on hereditary spastic paraplegia type 73 (spg73): Genetics This is caused by mutations in the CPT1C on chromosome 19q The transmission is autosomal dominant It usually presents as pure HSP The mean onset age is 36 years Clinical features Magnetic resonance…
Genetics
- This is caused by mutations in the CPT1C on chromosome 19q
- The transmission is autosomal dominant
- It usually presents as pure HSP
- The mean onset age is 36 years
Clinical features
Magnetic resonance imaging (MRI) brain
References
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