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1,037 Possible Causes for Severe Cerebellar Ataxia

  • Ataxia-Oculomotor Apraxia Syndrome

    Cerebellar ataxia with cerebellar atrophy on MRI and severe axonal sensorimotor neuropathy were present in all patients.[] […] a severe autosomal recessive progressive cerebellar ataxia, associated with oculocutaneous telangiectasia, abnormal eye movements, sinopulmonary disease, and immunodeficiency[] Examination of patient II-4 at 36 years revealed severe isolated cerebellar ataxia of his 4 limbs.[]

  • Acute Cerebellar Ataxia

    A 10-year-old girl exhibited severe cerebellar ataxia following acute enterocolitis, and was diagnosed as having acute cerebellar ataxia (ACA).[] We report the case of a 5-year-old girl seropositive for antibodies against the causative Lyme disease pathogen Borrelia burgdorferi presenting with severe acute cerebellar[] Furthermore, the extent of brain perfusion SPECT abnormalities correlated significantly with the clinical severity and the recovery time of cerebellar ataxia.[]

  • Cerebellar Ataxia

    The purpose of this case series is to describe changes in impairments and activity limitations in three individuals with severe cerebellar ataxia from traumatic brain injury[] Severity of cerebellar ataxia depends on the disease.[] Recognizing that anti-GAD-associated cerebellar ataxia can present in a young adult as an acute and severe cause of ataxia, with cerebellar changes evident on MRI.[]

  • Spinocerebellar Ataxia Type 6

    Clinically, SCA6 patients (n 12) presented with moderate to severe cerebellar ataxia with a lower frequency of associated signs compared with other SCA and a mean age at onset[] This relation was not correlated to other factors, such as age, education and severity of cerebellar ataxia, which are possible relevant factors associated with cognitive[] Spinocerebellar ataxia type 6 (SCA6) is the prototype of a pure cerebellar ataxia, associated with a severe form of progressive ataxia and cerebellar dysfunction.[]

  • Early-Onset Cerebellar Ataxia

    Evidence of atrophy did not correlate with either the duration of illness or the severity of cerebellar ataxia in both the groups.[] The patient displayed a severe phenotype with early onset cerebellar ataxia complicated by intellectual disability, epilepsy, attention deficit hyperactivity disorder, strabismus[] At the age of 10 years, clinical examination showed a severe cerebellar atactic gait, severe cerebellar limb ataxia, a clear cerebellar dysarthria and saccadic eye movements[]

  • Restless Legs Syndrome

    […] diseases such as multiple sclerosis, polyneuropathy, and cerebellar ataxias seem to be associated with the disorder ( Allen 2007 ; Connor 2008 ; Manconi 2004 ; Schöls 1998[] Beside the established causes of secondary RLS (e.g. end‐stage renal disease, pregnancy, and iron deficiency), an increasing number of conditions including several neurological[]

  • Posterior Cerebral Artery Occlusion with Infarction

    . - Occlusion of the superior cerebellar artery results in severe ipsilateral cerebellar ataxia, nausea and vomiting, dysarthria, and contralateral loss of pain and temperature[] . • Severe ipsilateral cerebellar ataxia • Nausea & vomitings • Dysarthria • Contralateral loss of pain & temperature over extremities, body & face. • Partial deafness, ataxic[] When stratified by infarction site, the frequency of gait ataxia is similar across all territories but tends to be most severe when the cerebellum and cerebellar tracts of[]

  • Orthostatic Hypotension

    […] or cerebellar findings Erectile dysfunction, constipation/diarrhea, urinary symptoms, decreased sweating are prevalent.[] , parkinsonism, & autonomic dysfunction Poor response to levodopa Severe orthostatic hypotension w/out compensatory tachycardia In multiple system atrophy: Extrapyramidal[] 3rd-5th decade, but may be later Multiple system atrophy (Shy-Drager syndrome) (OMIM 146500 ) COQ2 5 AR AD Adult-onset neurodegenerative disorder causing combination of ataxia[]

  • Infectious Mononucleosis

    Severe chronic active Epstein-Barr virus infection accompanied by virus-associated hemophagocytic syndrome, cerebellar ataxia and encephalitis.[]

  • Anxiety Disorder

    The clinical presentation deteriorates after several years, with neurological involvement (dementia, spastic paraparesis, cerebellar ataxia, convulsive seizures), optic nerve[] Table 1 Psychiatric manifestations of treatable hereditary metabolic disorders (general overview based on several cases from the literature) Schizophrenia Triggering factor[] ataxia, spastic paraplegia, dementia Cerebrotendinous xanthomatosis Chronic, late onset Hallucinations, behavioural disturbances ( ) Tetraplegia, spastic paraplegia, cerebellar[]

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