Cerebellar Ataxia [cerebelární ataxie]
- Terms
-
adiadochokineze
cerebelární hemiataxie
dysmetrie
hypermetrie
mozečková ataxie
-
Adiadochokinesis
Ataxia, Cerebellar
Cerebellar Dysmetria
Cerebellar Hemiataxia
Cerebellar Incoordination
Dysmetria
Hypermetria
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)
- Annotation
- DENTATE CEREBELLAR ATAXIA see MYOCLONIC CEREBELLAR DYSSYNERGIA is also available; ATAXIAS, HEREDITARY see SPINOCEREBELLAR DEGENERATION is also available
- DUI
- D002524 MeSH Browser
- CUI
- M0003856
- Previous indexing
- Ataxia (1966-1967); Cerebellar Diseases (1966-1967)
- History note
- 1968
- Public note
- 1968
Allowable subheadings
- BL
- blood 1
- CF
- cerebrospinal fluid
- CI
- chemically induced 2
- CL
- classification 3
- CO
- complications 4
- CN
- congenital
- DI
- diagnosis 28
- DG
- diagnostic imaging 1
- DH
- diet therapy 1
- DT
- drug therapy 1
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 21
- GE
- genetics 17
- HI
- history
- IM
- immunology 1
- ME
- metabolism 1
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 6
- PP
- physiopathology 9
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation 1
- SU
- surgery 4
- TH
- therapy 5
- UR
- urine
- VE
- veterinary 1
- VI
- virology
3-Methylglutaconic Aciduria, Type V Disease MeSH Browser
Aniridia cerebellar ataxia mental deficiency Disease MeSH Browser
Ataxia, Spastic, 1, Autosomal Dominant Disease MeSH Browser
Ataxia, Spastic, 3, Autosomal Recessive Disease MeSH Browser
Autosomal Recessive Cerebellar Ataxia Type 1 Disease MeSH Browser
Brachydactyly-Nystagmus-Cerebellar Ataxia Disease MeSH Browser
Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia Disease MeSH Browser
CANVAS syndrome Chemical MeSH Browser
CAPOS syndrome Disease MeSH Browser
Cerebellar Ataxia and Hypergonadotropic Hypogonadism Disease MeSH Browser
Cerebellar Ataxia and Hypogonadotropic Hypogonadism Disease MeSH Browser
Cerebellar Ataxia and Neurosensory Deafness Disease MeSH Browser
Cerebellar Ataxia, Benign, with Thermoanalgesia Disease MeSH Browser
Cerebellar Ataxia, Cayman Type Disease MeSH Browser
Cerebellar Ataxia, Deafness, and Narcolepsy Disease MeSH Browser
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Disease MeSH Browser
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Disease MeSH Browser
Cerebellar ataxia ectodermal dysplasia Disease MeSH Browser
Cerebellar hypoplasia with endosteal sclerosis Disease MeSH Browser
Dementia, familial Danish Disease MeSH Browser
Dysequilibrium syndrome Disease MeSH Browser
Episodic Ataxia, Type 5 Disease MeSH Browser
Episodic Ataxia, Type 6 Disease MeSH Browser
Furukawa Takagi Nakao syndrome Disease MeSH Browser
Hemiplegic migraine, familial type 1 Disease MeSH Browser
Herrmann syndrome Disease MeSH Browser
Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy Disease MeSH Browser
Mainzer-Saldino Disease Disease MeSH Browser
Marinesco-Sjogren-like syndrome (MSLS) Disease MeSH Browser
Myelocerebellar Disorder Disease MeSH Browser
Myoclonus, Cerebellar Ataxia, and Deafness Disease MeSH Browser
Neuhauser Eichner Opitz syndrome Disease MeSH Browser
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA Disease MeSH Browser