"Cerebellar Ataxia" 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.
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
| Descriptor ID |
D002524
|
| MeSH Number(s) |
C10.228.140.252.190 C10.597.350.090.500 C23.888.592.350.090.200
|
| Concept/Terms |
Cerebellar Ataxia- Cerebellar Ataxia
- Cerebellar Incoordination
- Cerebellar Incoordinations
- Incoordination, Cerebellar
- Incoordinations, Cerebellar
- Ataxia, Cerebellar
- Ataxias, Cerebellar
- Cerebellar Ataxias
Cerebellar Hemiataxia- Cerebellar Hemiataxia
- Cerebellar Hemiataxias
- Hemiataxia, Cerebellar
- Hemiataxias, Cerebellar
Cerebellar Dysmetria- Cerebellar Dysmetria
- Cerebellar Dysmetrias
- Dysmetria, Cerebellar
- Dysmetrias, Cerebellar
- Dysmetria
- Dysmetrias
|
Below are MeSH descriptors whose meaning is more general than "Cerebellar Ataxia".
Below are MeSH descriptors whose meaning is more specific than "Cerebellar Ataxia".
This graph shows the total number of publications written about "Cerebellar Ataxia" by people in this website by year, and whether "Cerebellar Ataxia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 |
| 2007 | 0 | 1 | 1 |
| 2016 | 1 | 1 | 2 |
| 2018 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cerebellar Ataxia" by people in Profiles.
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Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy. Genet Med. 2022 10; 24(10):2079-2090.
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Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development. Neuropediatrics. 2018 12; 49(6):379-384.
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Mesial temporal lobe epilepsy associated with KCNT1 mutation. Seizure. 2017 Feb; 45:181-183.
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Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome. PLoS One. 2016; 11(4):e0153757.
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Phenotypic characterization of hypomyelination and congenital cataract. Ann Neurol. 2007 Aug; 62(2):121-7.
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Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13. Am J Hum Genet. 1995 Jun; 56(6):1443-9.
MeSH information
