Conditions / Genetic
hereditary spastic paraplegia 16
info · Genetic · ICD-10: G11.4
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2.
Signs and symptoms
- Tetraplegia
- Facial hypotonia
- Strabismus
- Urinary urgency
- Babinski sign
- Shuffling gait
- Urinary incontinence
- Lower limb spasticity
- Lower limb muscle weakness
- Urinary bladder sphincter dysfunction
Also known as: SPG16; X-linked spastic paraplegia 16; X-linked spastic paraplegia type 16