A group of predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
Inga svenska synonymer finns.
Ataxia, Spinocerebellar — Ataxias, Spinocerebellar — Spinocerebellar Ataxia — Spinocerebellar Atrophies — Atrophies, Spinocerebellar — Atrophy, Spinocerebellar — Spinocerebellar Atrophy — Spinocerebellar Ataxia Type 1 — SCA1 — SCA1s — Spinocerebellar Ataxia-1 — Type 1 Spinocerebellar Ataxia — Schut-Haymaker Type OPCA — OPCA, Schut-Haymaker Type — Schut Haymaker Type OPCA — Spinocerebellar Atrophy I — Atrophy I, Spinocerebellar — Spinocerebellar Atrophy Is — Olivopontocerebellar Atrophy I — Atrophy I, Olivopontocerebellar — Olivopontocerebellar Atrophy Is — Cerebelloparenchymal Disorder I — Cerebelloparenchymal Disorder Is — Menzel Type OPCA — OPCA, Menzel Type — Olivopontocerebellar Atrophy IV — Atrophy IV, Olivopontocerebellar — Atrophy IVs, Olivopontocerebellar — Olivopontocerebellar Atrophy IVs — Spinocerebellar Ataxia 1 — Ataxia 1, Spinocerebellar — Spinocerebellar Ataxia 1s — Spinocerebellar Ataxia Type 7 — OPCA with Macular Degeneration and External Ophthalmoplegia — OPCA with Retinal Degeneration — Olivopontocerebellar Atrophy III — Atrophy III, Olivopontocerebellar — Olivopontocerebellar Atrophy IIIs — Spinocerebellar Ataxia-7 — Type 7 Spinocerebellar Ataxia — Spinocerebellar Ataxia 7 — Ataxia 7, Spinocerebellar — Spinocerebellar Ataxia 7s — Autosomal Dominant Cerebellar Ataxia, Type II — Spinocerebellar Ataxia Type 4 — Spinocerebellar Ataxia 4 — Ataxia 4, Spinocerebellar — Spinocerebellar Ataxia 4s — Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy — Spinocerebellar Ataxia-4 — Type 4 Spinocerebellar Ataxia — Spinocerebellar Ataxia Type 5 — Type 5 Spinocerebellar Ataxia — Spinocerebellar Ataxia 5 — Ataxia 5, Spinocerebellar — Spinocerebellar Ataxia 5s — Spinocerebellar Ataxia-5 — Spinocerebellar Ataxia Type 6 — Spinocerebellar Ataxia 6 — Ataxia 6, Spinocerebellar — Spinocerebellar Ataxia 6s — Spinocerebellar Ataxia-6 — Type 6 Spinocerebellar Ataxia — Dominantly-Inherited Spinocerebellar Ataxias — Ataxia, Dominantly-Inherited Spinocerebellar — Ataxias, Dominantly-Inherited Spinocerebellar — Dominantly Inherited Spinocerebellar Ataxias — Dominantly-Inherited Spinocerebellar Ataxia — Spinocerebellar Ataxia, Dominantly-Inherited — Spinocerebellar Ataxias, Dominantly-Inherited — Spinocerebellar Ataxias, Dominantly Inherited — Spinocerebellar Ataxia Type 2 — Cerebellar Degeneration with Slow Eye Movements — Olivopontocerebellar Atrophy 2 — Atrophy 2, Olivopontocerebellar — Atrophy 2s, Olivopontocerebellar — Olivopontocerebellar Atrophy 2s — Spinocerebellar Ataxia with Slow Eye Movements — Spinocerebellar Ataxia, Cuban Type — Spinocerebellar Atrophy 2 — Atrophy 2, Spinocerebellar — Atrophy 2s, Spinocerebellar — Spinocerebellar Atrophy 2s — Spinocerebellar Degeneration with Slow Eye Movements — Wadia Swami Syndrome — Swami Syndrome, Wadia — Syndrome, Wadia Swami — Olivopontocerebellar Atrophy, Holguin Type — Spinocerebellar Ataxia-2 — Type 2 Spinocerebellar Ataxia — Spinocerebellar Ataxia 2 — Ataxia 2, Spinocerebellar — Spinocerebellar Ataxia 2s — Wadia-Swami Syndrome — Syndrome, Wadia-Swami — Olivopontocerebellar Atrophy II — Atrophy II, Olivopontocerebellar — Olivopontocerebellar Atrophy IIs — Spinocerebellar Atrophy II — Atrophy IIs, Spinocerebellar — Spinocerebellar Atrophy IIs