Conditions / Genetic
hereditary spastic paraplegia 41
info · Genetic · ICD-10: G11.4
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.
Signs and symptoms
- Urinary urgency
- Lower limb muscle weakness
- Spastic gait
- Spastic paraplegia
- Hyperreflexia
Also known as: SPG41; autosomal dominant spastic paraplegia 41; autosomal dominant spastic paraplegia type 41