Conditions / Genetic
hereditary spastic paraplegia 92
info · Genetic
A hereditary spastic paraplegia that has_material_basis_in homozygous or compound heterozygous mutation in the FICD gene on chromosome 12q23.
Signs and symptoms
- Gait ataxia
- Intention tremor
- Lower limb muscle weakness
- Spastic paraparesis
- Memory impairment
- Postural tremor
- Limb ataxia
- Peripheral neuropathy
- Impaired distal vibration sensation
- Babinski sign
Also known as: SPG92; autosomal recessive spastic paraplegia 92