Autosomal recessive spastic paraplegia type 56

Orpha code: 320411OMIM code: 615030

Definition

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
Classification

Disease

Synonyms
SPG56
SPG56
ORPHA code
320411
OMIM code
615030
ICD10 code
G11.4
ICD11 code
-

No additional description.

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