ataxia

(redirected from limb ataxia)
Also found in: Thesaurus, Medical, Encyclopedia.
Related to limb ataxia: NIH Stroke Scale

a·tax·i·a

 (ə-tăk′sē-ə)
n.
1. Loss of the ability to coordinate muscular movement.
2. Any of various degenerative, often hereditary, disorders that are characterized by ataxia and are frequently associated with cerebellar atrophy.

[Greek ataxiā, disorder : a-, not; see a-1 + taxis, order.]

a·tax′ic adj. & n.

ataxia

(əˈtæksɪə) or

ataxy

n
(Pathology) pathol lack of muscular coordination
[C17: via New Latin from Greek: lack of coordination, from a-1 + -taxia, from tassein to put in order]
aˈtaxic, aˈtactic adj

a•tax•i•a

(əˈtæk si ə)

n.
loss of coordination of the muscles, esp. of the extremities.
[1605–15; < New Latin < Greek: indiscipline]
a•tax′ic, adj.

a·tax·i·a

(ə-tăk′sē-ə)
Loss of muscular coordination as a result of damage to the central nervous system.

ataxia, ataxy

inability to coordinate bodily movements, especially movements of the muscles. See also order and disorder.
See also: Disease and Illness
lack of order; irregularity. See also disease and illness.
See also: Order and Disorder

ataxia

Lack of coordination of the muscles.
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.ataxia - inability to coordinate voluntary muscle movements; unsteady movements and staggering gait
nervous disorder, neurological disease, neurological disorder - a disorder of the nervous system
Friedreich's ataxia, herediatry spinal ataxia - sclerosis of the posterior and lateral columns of the spinal cord; characterized by muscular weakness and abnormal gait; occurs in children
hereditary cerebellar ataxia - nervous disorder of late childhood and early adulthood; characterized by ataxic gait and hesitating or explosive speech and nystagmus
spinocerebellar disorder - any of several congenital disorders marked by degeneration of the cerebellum and spinal cord resulting in spasticity and ataxia
Translations
ataxie
ataksia

ataxia

[əˈtæksɪə] Nataxia f

ataxia

nAtaxie f

ataxia

n ataxia
References in periodicals archive ?
sup][3],[4] The cardinal clinical characteristics of SCA3 include gait and stance unsteadiness, limb ataxia, dysarthria, oculomotor dysfunction, sensory disorder, pyramidal and extrapyramidal dysfunction, and so on.
In MFS, most patients initially have ophthalmoplegia followed by gait and limb ataxia.
Six months after illness onset, he experienced hallucinations, weakness of lower extremities, and limb ataxia.