Conditions / Genetic
hereditary spastic paraplegia 32
info · Genetic · ICD-10: G11.4
A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.
Signs and symptoms
- Cerebral atrophy
- Mild intellectual disability
- Pes cavus
- Gait disturbance
- Babinski sign
- Hypoplasia of the corpus callosum
- Cerebellar atrophy
- Spastic gait
- Lower limb spasticity
- Ankle clonus
Also known as: SPG32; autosomal recessive spastic paraplegia 32; autosomal recessive spastic paraplegia type 32