Autosomal dominant spastic paraplegia type 38

Orpha code: 171617OMIM code: 612335

Definicja

A complex hereditary spastic paraplegia characterized by mild to severe lower limb spasticity, hyperreflexia, extensor plantar responses, impaired vibration sensation, <i>pes cavus</i>, and significant wasting and weakness of the small hand muscles. Temporal lobe epilepsy and cognitive dysfunction have been also reported.

Disease data
Klasyfikacja

Disease

Synonimy
SPG38
SPG38
Kod ORPHA
171617
Kod OMIM
612335
Kod ICD10
G11.4
Kod ICD11
8B44.00

No additional description.

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