Spastic paraplegia-74 (SPG74) is an autosomal recessive neurologic disorder characterized by onset of slowly progressive lower limb spasticity, optic atrophy, and peripheral neuropathy in the first decade (summary by Lossos et al., 2015).
For a discussion of genetic heterogeneity of autosomal recessive spastic paraplegia, see SPG5A (270800). [from
OMIM]