Conditions / Genetic
hereditary spastic paraplegia 37
info · Genetic · ICD-10: G11.4
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 8p21.1-q13.3.
Signs and symptoms
- Urinary urgency
- Lower limb hyperreflexia
- Urinary incontinence
- Spastic gait
- Lower limb spasticity
- Spastic paraplegia
- Impaired vibration sensation in the lower limbs
- Babinski sign
- Ankle clonus
- Upper limb hyperreflexia
Also known as: SPG37; autosomal dominant spastic paraplegia 37; autosomal dominant spastic paraplegia type 37