Autosomal dominant spastic paraplegia type 36

Orpha code: 320365OMIM code: 613096

Definition

A complex form of hereditary spastic paraplegia, characterized by an onset in childhood or adulthood of progressive spastic paraplegia (with spastic gait, spasticity, lower limb weakness, pes cavus and urinary urgency) associated with the additional manifestation of peripheral sensorimotor neuropathy.

Disease data
Classification

Disease

Synonyms
SPG36
SPG36
ORPHA code
320365
OMIM code
613096
ICD10 code
G11.4
ICD11 code
-

No additional description.

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