Spinocerebellar Ataxias
Synonyms
Ataxia 1, Spinocerebellar
Ataxia 2, Spinocerebellar
Ataxia 2s, Spinocerebellar
Ataxia 4, Spinocerebellar
Ataxia 4s, Spinocerebellar
Ataxia 5, Spinocerebellar
Ataxia 5s, Spinocerebellar
Ataxia 6, Spinocerebellar
Ataxia 6s, Spinocerebellar
Ataxia 7, Spinocerebellar
Ataxia 7s, Spinocerebellar
Ataxia, Dominantly-Inherited Spinocerebellar
Ataxia, Spinocerebellar
Ataxias, Dominantly-Inherited Spinocerebellar
Ataxias, Spinocerebellar
Atrophies, Spinocerebellar
Atrophy 2, Olivopontocerebellar
Atrophy 2, Spinocerebellar
Atrophy 2s, Olivopontocerebellar
Atrophy 2s, Spinocerebellar
Atrophy I, Olivopontocerebellar
Atrophy I, Spinocerebellar
Atrophy II, Olivopontocerebellar
Atrophy II, Spinocerebellar
Atrophy III, Olivopontocerebellar
Atrophy IIs, Olivopontocerebellar
Atrophy IIs, Spinocerebellar
Atrophy IV, Olivopontocerebellar
Atrophy IVs, Olivopontocerebellar
Atrophy, Spinocerebellar
Autosomal Dominant Cerebellar Ataxia, Type II
Cerebellar Degeneration with Slow Eye Movements
Cerebelloparenchymal Disorder I
Cerebelloparenchymal Disorder Is
Dominantly Inherited Spinocerebellar Ataxias
Dominantly-Inherited Spinocerebellar Ataxia
Dominantly-Inherited Spinocerebellar Ataxias
II, Olivopontocerebellar Atrophy
II, Spinocerebellar Atrophy
IIs, Olivopontocerebellar Atrophy
IIs, Spinocerebellar Atrophy
Menzel Type OPCA
OPCA with Macular Degeneration and External Ophthalmoplegia
OPCA with Retinal Degeneration
OPCA, Menzel Type
OPCA, Schut-Haymaker Type
Olivopontocerebellar Atrophy 2
Olivopontocerebellar Atrophy 2s
Olivopontocerebellar Atrophy I
Olivopontocerebellar Atrophy II
Olivopontocerebellar Atrophy III
Olivopontocerebellar Atrophy IIIs
Olivopontocerebellar Atrophy IIs
Olivopontocerebellar Atrophy IV
Olivopontocerebellar Atrophy IVs
Olivopontocerebellar Atrophy Is
Olivopontocerebellar Atrophy, Holguin Type
SCA1
SCA1s
Schut Haymaker Type OPCA
Schut-Haymaker Type OPCA
Spinocerebellar Ataxia
Spinocerebellar Ataxia 1
Spinocerebellar Ataxia 1s
Spinocerebellar Ataxia 2
Spinocerebellar Ataxia 2s
Spinocerebellar Ataxia 4
Spinocerebellar Ataxia 4s
Spinocerebellar Ataxia 5
Spinocerebellar Ataxia 5s
Spinocerebellar Ataxia 6
Spinocerebellar Ataxia 6s
Spinocerebellar Ataxia 7
Spinocerebellar Ataxia 7s
Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 6
Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia with Slow Eye Movements
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
Spinocerebellar Ataxia, Cuban Type
Spinocerebellar Ataxia, Dominantly-Inherited
Spinocerebellar Ataxia-1
Spinocerebellar Ataxia-2
Spinocerebellar Ataxia-4
Spinocerebellar Ataxia-5
Spinocerebellar Ataxia-6
Spinocerebellar Ataxia-7
Spinocerebellar Ataxias, Dominantly Inherited
Spinocerebellar Ataxias, Dominantly-Inherited
Spinocerebellar Atrophies
Spinocerebellar Atrophy
Spinocerebellar Atrophy 2
Spinocerebellar Atrophy 2s
Spinocerebellar Atrophy I
Spinocerebellar Atrophy II
Spinocerebellar Atrophy IIs
Spinocerebellar Atrophy Is
Spinocerebellar Degeneration with Slow Eye Movements
Swami Syndrome, Wadia
Syndrome, Wadia Swami
Syndrome, Wadia-Swami
Type 1 Spinocerebellar Ataxia
Type 2 Spinocerebellar Ataxia
Type 4 Spinocerebellar Ataxia
Type 5 Spinocerebellar Ataxia
Type 6 Spinocerebellar Ataxia
Type 7 Spinocerebellar Ataxia
Wadia Swami Syndrome
Wadia-Swami Syndrome
A group of dominantly inherited, 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)