PNPLA6-related spastic paraplegia with or without ataxia

An autosomal recessive, multisystem condition caused by pathogenic variants of the PNPLA6 gene that characterized by peripheral neuropathy, cognitive impairment, lower limb spasticity, muscle weakness, and reduced vibration sense. Additional clinical features may include cerebellar ataxia, hypogonadism, growth hormone deficiency, and hypothyroidism.

2 clinical trials for this condition and its sub-types, 0 tagged with PNPLA6-related spastic paraplegia with or without ataxia itself.