X-linked spastic paraplegia type 16

Orpha code: 100997OMIM code: 300266

Definition

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
Classification

Disease

Synonyms
SPG16
SPG16
ORPHA code
100997
OMIM code
300266
ICD10 code
G11.4
ICD11 code
-

No additional description.

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