Autosomal recessive spastic paraplegia type 56

Orpha code: 320411OMIM code: 615030

Definicja

A rare form of hereditary spastic paraplegia characterized by delayed walking, toe walking, unsteady and spastic gait, hyperreflexia of the lower limbs, and extensor plantar responses. Upper limbs spasticity and dystonia, subclinical axonal neuropathy, cognitive impairment and intellectual disability have also been associated.

Disease data
Klasyfikacja

Disease

Synonimy
SPG56
SPG56
Kod ORPHA
320411
Kod OMIM
615030
Kod ICD10
G11.4
Kod ICD11
-

No additional description.

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