 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 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 Ataxias, Dominantly-Inherited
- Spinocerebellar Ataxias, Dominantly Inherited
Spinocerebellar Ataxia Type 5- Spinocerebellar Ataxia Type 5
- Spinocerebellar Ataxia-5
- Type 5 Spinocerebellar Ataxia
- Spinocerebellar Ataxia 5
- 5, Spinocerebellar Ataxia
- 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 2- Spinocerebellar Ataxia Type 2
- Wadia-Swami Syndrome
- Syndrome, Wadia-Swami
- Spinocerebellar Ataxia-2
- Type 2 Spinocerebellar Ataxia
- Cerebellar Degeneration with Slow Eye Movements
- Spinocerebellar Ataxia 2
- Ataxia 2, Spinocerebellar
- Ataxia 2s, Spinocerebellar
- Spinocerebellar Ataxia 2s
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
Spinocerebellar Ataxia Type 7- Spinocerebellar Ataxia Type 7
- OPCA with Macular Degeneration and External Ophthalmoplegia
- OPCA with Retinal Degeneration
- Olivopontocerebellar Atrophy III
- Atrophy III, Olivopontocerebellar
- Olivopontocerebellar Atrophy IIIs
- Type 7 Spinocerebellar Ataxia
- Autosomal Dominant Cerebellar Ataxia, Type II
- Spinocerebellar Ataxia-7
- Spinocerebellar Ataxia 7
- Ataxia 7, Spinocerebellar
- Ataxia 7s, Spinocerebellar
- Spinocerebellar Ataxia 7s
Spinocerebellar Ataxia Type 1- Spinocerebellar Ataxia Type 1
- Menzel Type OPCA
- OPCA, Menzel Type
- Olivopontocerebellar Atrophy I
- Atrophy I, Olivopontocerebellar
- Olivopontocerebellar Atrophy Is
- Olivopontocerebellar Atrophy IV
- Spinocerebellar Ataxia 1
- Ataxia 1, Spinocerebellar
- Spinocerebellar Ataxia 1s
- Spinocerebellar Ataxia-1
- Spinocerebellar Atrophy I
- Atrophy I, Spinocerebellar
- Spinocerebellar Atrophy Is
- Type 1 Spinocerebellar Ataxia
- Cerebelloparenchymal Disorder I
- Cerebelloparenchymal Disorder Is
- Schut-Haymaker Type OPCA
- OPCA, Schut-Haymaker Type
- Schut Haymaker Type OPCA
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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 UAMS Profiles by year, and whether "Spinocerebellar Ataxias" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
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| 2024 | 0 | 1 | 1 | | 2022 | 1 | 0 | 1 | | 2007 | 1 | 0 | 1 |
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Below are the most recent publications written about "Spinocerebellar Ataxias" by people in Profiles over the past ten years.
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Benkirane M, Bonhomme M, Morsy H, Safgren SL, Marelli C, Chaussenot A, Smedley D, Cipriani V, de Sainte-Agathe JM, Ding C, Larrieu L, Vestito L, Margot H, Lesca G, Ramond F, Castrioto A, Baux D, Verheijen J, Sansa E, Giunti P, Haetty A, Bergougnoux A, Pointaux M, Ardouin O, Van Goethem C, Vincent MC, Hadjivassiliou M, Coss?e M, Rouaud T, Bartsch O, Freeman WD, Wierenga KJ, Klee EW, Vandrovcova J, Houlden H, Debant A, Koenig M. De novo and inherited monoallelic variants in TUBA4A cause ataxia and spasticity. Brain. 2024 Nov 04; 147(11):3681-3689.
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Louie SM, Moye AL, Wong IG, Lu E, Shehaj A, Garcia-de-Alba C, Ararat E, Raby BA, Lu B, Paschini M, Bronson RT, Kim CF. Progenitor potential of lung epithelial organoid cells in a transplantation model. Cell Rep. 2022 04 12; 39(2):110662.
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