Autosomal dominant spastic paraplegia type 37

Orpha code: 171612OMIM code: 611945

Definicja

A pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients.

Disease data
Klasyfikacja

Disease

Synonimy
SPG37
SPG37
Kod ORPHA
171612
Kod OMIM
611945
Kod ICD10
G11.4
Kod ICD11
8B44.00

No additional description.

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