Spinocerebellar Ataxias
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)
Year introduced: 2000
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Tree Number(s): C10.228.140.252.190.530, C10.228.140.252.700.700, C10.228.854.787.875, C10.574.500.825.700, C10.597.350.090.500.530, C16.320.400.780.875
MeSH Unique ID: D020754
Entry Terms:
- 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
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