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X-linked spastic paraplegia type 16

ORPHA:100997· ICD-10 G11.4

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.

Prevalence
<1 / 1 000 000
Inheritance
X-linked recessive
Age of onset
Infancy