Conditions / Genetic
hereditary spastic paraplegia 29
info · Genetic · ICD-10: G11.4
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1.
Signs and symptoms
- Hiatus hernia
- Clonus
- Urinary urgency
- Pes cavus
- Vomiting
- Babinski sign
- Impaired vibratory sensation
- Neonatal hyperbilirubinemia
- Urinary incontinence
- Lower limb spasticity
Also known as: SPG29; autosomal dominant spastic paraplegia 29