Conditions / Genetic
hereditary spastic paraplegia 75
info · Genetic · ICD-10: G11.4
A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13.
Signs and symptoms
- Astigmatism
- Spastic dysarthria
- Hypermetropia
- Dysmetria
- Hypotonia
- Spastic gait
- Nystagmus
- Reduced visual acuity
- Spastic paraparesis
- Hyperreflexia
Also known as: SPG75; autosomal recessive spastic paraplegia 75; autosomal recessive spastic paraplegia type 75