 Olivopontocerebellar Atrophies
"Olivopontocerebellar Atrophies" 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 inherited and sporadic disorders which share progressive ataxia in combination with atrophy of the CEREBELLUM; PONS; and inferior olivary nuclei. Additional clinical features may include MUSCLE RIGIDITY; NYSTAGMUS, PATHOLOGIC; RETINAL DEGENERATION; MUSCLE SPASTICITY; DEMENTIA; URINARY INCONTINENCE; and OPHTHALMOPLEGIA. The familial form has an earlier onset (second decade) and may feature spinal cord atrophy. The sporadic form tends to present in the fifth or sixth decade, and is considered a clinical subtype of MULTIPLE SYSTEM ATROPHY. (From Adams et al., Principles of Neurology, 6th ed, p1085)
| Descriptor ID |
D009849
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| MeSH Number(s) |
C10.177.575.550.375 C10.228.140.079.612.600 C10.228.140.252.700.650 C10.228.662.550.600 C10.228.854.787.750 C10.574.500.825.650 C10.574.625.600 C16.320.400.780.750
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| Concept/Terms |
Olivopontocerebellar Atrophies- Olivopontocerebellar Atrophies
- Olivopontocerebellar Atrophy
- Atrophy, Olivopontocerebellar
- Olivo-Ponto-Cerebellar Atrophy
- Atrophy, Olivo-Ponto-Cerebellar
- Olivo Ponto Cerebellar Atrophy
- Dejerine-Thomas Syndrome
- Dejerine Thomas Syndrome
- Syndrome, Dejerine-Thomas
- Presenile Ataxia
- Ataxia, Presenile
- Ataxias, Presenile
- Presenile Ataxias
- Pontoolivocerebellar Atrophy
- Atrophy, Pontoolivocerebellar
- Pontoolivocerebellar Atrophies
- Olivopontocerebellar Degeneration
- Degeneration, Olivopontocerebellar
- Degenerations, Olivopontocerebellar
- Olivopontocerebellar Degenerations
- Olivo-Ponto-Cerebellar Degeneration
- Degeneration, Olivo-Ponto-Cerebellar
- Degenerations, Olivo-Ponto-Cerebellar
- Olivo Ponto Cerebellar Degeneration
- Olivo-Ponto-Cerebellar Degenerations
Olivopontocerebellar Atrophy, Idiopathic- Olivopontocerebellar Atrophy, Idiopathic
- Atrophy, Idiopathic Olivopontocerebellar
- Idiopathic Olivopontocerebellar Atrophies
- Idiopathic Olivopontocerebellar Atrophy
- Olivopontocerebellar Atrophies, Idiopathic
Familial Olivopontocerebellar Atrophy- Familial Olivopontocerebellar Atrophy
- Atrophy, Familial Olivopontocerebellar
- Familial Olivopontocerebellar Atrophies
- Olivopontocerebellar Atrophies, Familial
- Olivopontocerebellar Atrophy, Familial
- Inherited Olivopontocerebellar Atrophy
- Atrophy, Inherited Olivopontocerebellar
- Inherited Olivopontocerebellar Atrophies
- Olivopontocerebellar Atrophies, Inherited
- Olivopontocerebellar Atrophy, Inherited
Nonfamilial Olivopontocerebellar Atrophy- Nonfamilial Olivopontocerebellar Atrophy
- Atrophy, Nonfamilial Olivopontocerebellar
- Nonfamilial Olivopontocerebellar Atrophies
- Olivopontocerebellar Atrophies, Nonfamilial
- Olivopontocerebellar Atrophy, Nonfamilial
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Below are MeSH descriptors whose meaning is more general than "Olivopontocerebellar Atrophies".
Below are MeSH descriptors whose meaning is more specific than "Olivopontocerebellar Atrophies".
This graph shows the total number of publications written about "Olivopontocerebellar Atrophies" by people in this website by year, and whether "Olivopontocerebellar Atrophies" 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 |
|---|
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Olivopontocerebellar Atrophies" by people in Profiles.
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Rosenblum JS, Nazari M, Al-Khalili Y, Potigailo V, Veznedaroglu E. Unilateral Symptomatic Hypertrophic Olivary Degeneration Secondary to Midline Brainstem Cavernous Angioma: A Case Report and Review of the Literature. World Neurosurg. 2018 Feb; 110:294-300.
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Rudnik-Sch?neborn S, Senderek J, Jen JC, Houge G, Seeman P, Puchmajerov? A, Graul-Neumann L, Seidel U, Korinthenberg R, Kirschner J, Seeger J, Ryan MM, Muntoni F, Steinlin M, Sztriha L, Colomer J, H?bner C, Brockmann K, Van Maldergem L, Schiff M, Holzinger A, Barth P, Reardon W, Yourshaw M, Nelson SF, Eggermann T, Zerres K. Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations. Neurology. 2013 Jan 29; 80(5):438-46.
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Wan J, Yourshaw M, Mamsa H, Rudnik-Sch?neborn S, Menezes MP, Hong JE, Leong DW, Senderek J, Salman MS, Chitayat D, Seeman P, von Moers A, Graul-Neumann L, Kornberg AJ, Castro-Gago M, Sobrido MJ, Sanefuji M, Shieh PB, Salamon N, Kim RC, Vinters HV, Chen Z, Zerres K, Ryan MM, Nelson SF, Jen JC. Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration. Nat Genet. 2012 Apr 29; 44(6):704-8.
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