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