X-linked spastic paraplegia type 16

Orpha code: 100997OMIM code: 300266

Definicja

A complex, hereditary, spastic paraplegia characterized by delayed motor development, spasticity, and inability to walk, later progressing to quadriplegia, motor aphasia, bowel and bladder dysfunction. Patients also present with vision problems and mild intellectual disability. The disease affects only males.

Disease data
Klasyfikacja

Disease

Synonimy
SPG16
SPG16
Kod ORPHA
100997
Kod OMIM
300266
Kod ICD10
G11.4
Kod ICD11
-

No additional description.

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