Autosomal recessive spastic paraplegia type 59

Orpha code: 401795OMIM code:

Definition

Autosomal recessive spastic paraplegia type 59 is a very rare, complex hereditary spastic paraplegia characterized by an early onset of progressive lower limb spasticity, tip-toe walking, scissor gait, hyperreflexia and clonus that may be associated with borderline intellectual disability. Nystagmus and pes equinovarus have also been reported.

Disease data
Classification

Disease

Synonyms
SPG59
SPG59
ORPHA code
401795
OMIM code
-
ICD10 code
G11.4
ICD11 code
-

No additional description.

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