Autosomal dominant spastic paraplegia type 12

Orpha code: 100993OMIM code: 604805

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.

Disease data
Classification

Disease

Synonyms
SPG12
SPG12
ORPHA code
100993
OMIM code
604805
ICD10 code
G11.4
ICD11 code
-

No additional description.

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