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- W4282023243 abstract "Ataxia is derived from the Greek meaning lack of order or coordination – features seen typically in diseases of the cerebellum and its connections. Acute cerebellar ataxia of childhood is post-infective. Chronic abuse can produce progressive gait and limb ataxia with dysarthria. Neuropathy is frequently present. Multiple system atrophy can present with a parkinsonian syndrome, with autonomic dysfunction or as a cerebellar syndrome. Friedreich's Ataxia is characterised by progressive gait and limb ataxia, axonal sensorimotor neuropathy, pyramidal tract involvement, hypertrophic cardiomyopathy, skeletal abnormalities, optic atrophy, deafness and diabetes, typically evident between 8 and 15 years. Ataxia telangiectasia (AT) is a movement disorder with progressive ataxia, dystonia and chorea. AT is associated with defective humoral and cell-mediated immunity and is caused by ataxia telangiectasia mutated gene mutations. Ataxic syndromes associated with X chromosome mutations are rare." @default.
- W4282023243 created "2022-06-13" @default.
- W4282023243 date "2022-05-27" @default.
- W4282023243 modified "2023-10-16" @default.
- W4282023243 title "Ataxias, Cerebellar Disorders and Related Conditions" @default.
- W4282023243 cites W1549405276 @default.
- W4282023243 doi "https://doi.org/10.1002/9781119235699.ch17" @default.
- W4282023243 hasPublicationYear "2022" @default.
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