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)
推出的年份: 2000
树号: 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 单一 ID: D020754
进入的组:
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
早前的内容:
Ataxia/genetics (1965-1999)
Cerebellar Diseases (1966-1999)
Spinal Cord Diseases (1966-1999)
Spinocerebellar Degenerations (1987-1999)
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