Spastic paraplegia 12
Alternate names
SPG12
Definition
A pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus.
NIH genetic and rare disease info
Spastic paraplegia 12 is a rare disease.
Resources
Frequently asked questions
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