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

NIH info on Spastic paraplegia 12

Spastic paraplegia 12 is a rare disease.

Resources

Frequently asked questions

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Spastic paraplegia 12
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