Spinocerebellar Ataxias
"Spinocerebellar Ataxias" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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)
Descriptor ID |
D020754
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MeSH 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
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Concept/Terms |
Spinocerebellar Ataxias- Spinocerebellar Ataxias
- Ataxia, Spinocerebellar
- Ataxias, Spinocerebellar
- Spinocerebellar Ataxia
- Spinocerebellar Ataxias, Dominantly-Inherited
- Spinocerebellar Ataxias, Dominantly Inherited
- Spinocerebellar Atrophies
- Atrophies, Spinocerebellar
- Atrophy, Spinocerebellar
- Spinocerebellar Atrophy
- 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 Ataxia Type 2- Spinocerebellar Ataxia Type 2
- Olivopontocerebellar Atrophy 2
- Atrophy 2, Olivopontocerebellar
- Atrophy 2s, Olivopontocerebellar
- Olivopontocerebellar Atrophy 2s
- Olivopontocerebellar Atrophy II
- Olivopontocerebellar Atrophy, Holguin Type
- Spinocerebellar Ataxia 2
- Ataxia 2, Spinocerebellar
- Ataxia 2s, Spinocerebellar
- Spinocerebellar Ataxia 2s
- Spinocerebellar Ataxia with Slow Eye Movements
- Spinocerebellar Ataxia, Cuban Type
- Spinocerebellar Ataxia-2
- Spinocerebellar Atrophy 2
- Atrophy 2, Spinocerebellar
- Atrophy 2s, Spinocerebellar
- Spinocerebellar Atrophy 2s
- Spinocerebellar Atrophy II
- Spinocerebellar Degeneration with Slow Eye Movements
- Type 2 Spinocerebellar Ataxia
- Wadia Swami Syndrome
- Swami Syndrome, Wadia
- Syndrome, Wadia Swami
- Wadia-Swami Syndrome
- Syndrome, Wadia-Swami
- Cerebellar Degeneration with Slow Eye Movements
Spinocerebellar Ataxia Type 7- Spinocerebellar Ataxia Type 7
- Olivopontocerebellar Atrophy III
- Atrophy III, Olivopontocerebellar
- Olivopontocerebellar Atrophy IIIs
- Type 7 Spinocerebellar Ataxia
- OPCA with Retinal Degeneration
- Spinocerebellar Ataxia 7
- Ataxia 7, Spinocerebellar
- Ataxia 7s, Spinocerebellar
- Spinocerebellar Ataxia 7s
- Spinocerebellar Ataxia-7
- Autosomal Dominant Cerebellar Ataxia, Type II
- OPCA with Macular Degeneration and External Ophthalmoplegia
Spinocerebellar Ataxia Type 5- Spinocerebellar Ataxia Type 5
- Spinocerebellar Ataxia-5
- Type 5 Spinocerebellar Ataxia
- Spinocerebellar Ataxia 5
- Ataxia 5, Spinocerebellar
- Ataxia 5s, Spinocerebellar
- Spinocerebellar Ataxia 5s
Spinocerebellar Ataxia Type 6- Spinocerebellar Ataxia Type 6
- Spinocerebellar Ataxia-6
- Type 6 Spinocerebellar Ataxia
- Spinocerebellar Ataxia 6
- Ataxia 6, Spinocerebellar
- Ataxia 6s, Spinocerebellar
- Spinocerebellar Ataxia 6s
Spinocerebellar Ataxia Type 1- Spinocerebellar Ataxia Type 1
- Type 1 Spinocerebellar Ataxia
- Cerebelloparenchymal Disorder I
- Cerebelloparenchymal Disorder Is
- Menzel Type OPCA
- OPCA, Menzel Type
- Spinocerebellar Ataxia-1
- Olivopontocerebellar Atrophy IV
- Atrophy IV, Olivopontocerebellar
- Atrophy IVs, Olivopontocerebellar
- Olivopontocerebellar Atrophy IVs
- SCA1
- Schut-Haymaker Type OPCA
- OPCA, Schut-Haymaker Type
- Schut Haymaker Type OPCA
- Spinocerebellar Ataxia 1
- Ataxia 1, Spinocerebellar
- Spinocerebellar Ataxia 1s
- Spinocerebellar Atrophy I
- Atrophy I, Spinocerebellar
- Spinocerebellar Atrophy Is
- Olivopontocerebellar Atrophy I
- Atrophy I, Olivopontocerebellar
- Olivopontocerebellar Atrophy Is
Spinocerebellar Ataxia Type 4- Spinocerebellar Ataxia Type 4
- Type 4 Spinocerebellar Ataxia
- Spinocerebellar Ataxia-4
- Spinocerebellar Ataxia 4
- Ataxia 4, Spinocerebellar
- Ataxia 4s, Spinocerebellar
- Spinocerebellar Ataxia 4s
- Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
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Below are MeSH descriptors whose meaning is more general than "Spinocerebellar Ataxias".
Below are MeSH descriptors whose meaning is more specific than "Spinocerebellar Ataxias".
This graph shows the total number of publications written about "Spinocerebellar Ataxias" by people in this website by year, and whether "Spinocerebellar Ataxias" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2012 | 1 | 0 | 1 | 2015 | 1 | 0 | 1 | 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Spinocerebellar Ataxias" by people in Profiles.
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Perez-Lloret S, van de Warrenburg B, Rossi M, Rodríguez-Blázquez C, Zesiewicz T, Saute JAM, Durr A, Nishizawa M, Martinez-Martin P, Stebbins GT, Schrag A, Skorvanek M. Assessment of Ataxia Rating Scales and Cerebellar Functional Tests: Critique and Recommendations. Mov Disord. 2021 02; 36(2):283-297.
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Keiser MS, Kordower JH, Gonzalez-Alegre P, Davidson BL. Broad distribution of ataxin 1 silencing in rhesus cerebella for spinocerebellar ataxia type 1 therapy. Brain. 2015 Dec; 138(Pt 12):3555-66.
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Kapur SS, Goldman JG. Two in one: report of a patient with spinocerebellar ataxia types 2 and 10. Arch Neurol. 2012 Sep; 69(9):1200-3.
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