A severe neurologic disorder characterized by the onset of intractable myoclonic seizures soon after birth.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
hereditary spastic paraplegia 10
MONDO:0011408
autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
MONDO:0017940