Autosomal dominant spastic paraplegia type 19

Orpha code: 100999OMIM code: 607152

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.

Disease data
Classification

Disease

Synonyms
SPG19
SPG19
ORPHA code
100999
OMIM code
607152
ICD10 code
G11.4
ICD11 code
-

No additional description.

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