Autosomal recessive spastic paraplegia type 62

Orpha code: 401785OMIM code: 615681

Definicja

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
Klasyfikacja

Disease

Synonimy
SPG62
SPG62
Kod ORPHA
401785
Kod OMIM
615681
Kod ICD10
G11.4
Kod ICD11
-

No additional description.

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