Autosomal recessive spastic paraplegia type 62

Orpha code: 401785OMIM code: 615681

Definition

A pure or complex form of hereditary spastic paraplegia characterized by an onset in the first decade of life of spastic paraperesis (more prominent in lower than upper extremities) and unsteady gait, as well as increased deep tendon reflexes, amyotrophy, cerebellar ataxia, and flexion contractures of the knees, in some.

Disease data
Classification

Disease

Synonyms
SPG62
SPG62
ORPHA code
401785
OMIM code
615681
ICD10 code
G11.4
ICD11 code
-

No additional description.

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