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Autosomal dominant spastic paraplegia type 19

ORPHA:100999· ICD-10 G11.4

Definition

A pure form of hereditary spastic paraplegia characterized by a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal dominant
Age of onset
Adult