Hereditary spastic paraplegia 2

Spastic paraplegia type 2 (SPG2) is an X-linked leukodystrophy characterized primarily by spastic gait and autonomic dysfunction. When additional central nervous system (CNS) signs, such as intellectual deficit, ataxia, or extrapyramidal signs, are present, the syndrome is referred to as complicated SPG.

Also known as: PLP1 hereditary spastic paraplegia, SPG2, X-linked spastic paraplegia type 2, hereditary spastic paraplegia caused by mutation in PLP1, hereditary spastic paraplegia type 2, spastic gait type 2, spastic paraparesis type 2, spastic paraplegia 2, X-linked, X-linked recessive

2 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spastic paraplegia 2 itself.