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466 Possible Causes for Adult Onset Cerebellar Ataxia

  • Knobloch Syndrome Type 1

    […] foveomacular vitelliform dystrophy Alström syndrome Amaurosis-hypertrichosis syndrome Aniridia Aniridia-absent patella syndrome Aniridia-cerebellar ataxia-intellectual disability[] Ablepharon macrostomia syndrome Abnormal eye movements Aceruloplasminemia Achromatopsia Acute annular outer retinopathy Acute endophthalmitis Acute zonal occult outer retinopathy Adult-onset[]

  • Cerebellar Ataxia

    To conclude, ALD accounts for approximately 0.39% (2/516) of adult-onset cerebellar ataxias.[] This report suggests the importance of investigating mitochondrial function and, in particular, muscle CoQ10 levels, in patients with adult-onset cerebellar ataxia.[] Abstract Autosomal Recessive Cerebellar Ataxia type 1 (ARCA1), also known as recessive ataxia of Beauce, is an adult onset pure cerebellar ataxia that typically presents with[]

  • Vitamin B12 Deficiency

    Acute onset of cerebellar dysfunction and extrapyramidal manifestations like dystonia and chorea are rather uncommon in adults.[] We describe a patient who manifested with acute onset of language dysfunction, chorea and ataxia.[]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    We suggest CLN genes should be considered in the molecular analyses of patients presenting with adult-onset autosomal recessive cerebellar ataxia.[] Our findings support CLN5 hypomorphic mutations cause autosomal recessive cerebellar ataxia, confirming other reports showing CLN mutations are associated with adult-onset[]

  • Neuropathy

    Adult onset cerebellar dysfunction with neuropathy is a commonly encountered condition and is usually due to genetic causes such as spinocerebellar ataxia, gluten ataxia,[]

  • Orthostatic Hypotension

    […] anhidrosis; urinary retention or incontinence Onset typically in 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, parkinsonism, & autonomic dysfunction Poor response to levodopa Severe orthostatic hypotension w/out compensatory[] […] tachycardia In multiple system atrophy: Extrapyramidal or cerebellar findings Erectile dysfunction, constipation/diarrhea, urinary symptoms, decreased sweating are prevalent[]

  • Spinocerebellar Ataxia Type 13

    […] by progressive ataxia and progressive cerebellar degeneration.[] To test the hypothesis that infant- and adult-onset mutations have differential effects on neuronal development… CONTINUE READING From This Paper Figures, tables, and topics[] […] by progressive ataxia and cerebellar degeneration.[]

  • Hereditary Late-Onset Parkinson Disease

    Abstract Multiple system atrophy (MSA) is a progressive, adult-onset, neurodegenerative disorder characterized by parkinsonism, cerebellar ataxia, autonomic failure, and corticospinal[] In clinical practice, it is often advisable to test for SCA mutations when evaluating patients presenting with adult-onset cerebellar ataxia, with or without a known family[] However, there is one case report of a patient with adult-onset cerebellar ataxia with dysautonomia and parkinsonism who was clinically diagnosed with MSA, who subsequently[]

  • Diarrhea

    Gluten sensitivity in Japanese patients with adult-onset cerebellar ataxia. Intern Med. 2006; 45 :135–40. [ PubMed ] [ Google Scholar ] 195.[]

  • Laryngeal Abductor Paralysis

    […] familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy. ( 11376202 ) Barbieri F....De Michele G. 2001 5 Localization of the gene for familial[] 17826894 ) Deguchi K....Kuriyama S. 2007 3 Laryngeal abductor paralysis can be a solitary manifestation of multiple system atrophy. ( 15946984 ) Uzawa A....Hattori T. 2005 4 Adult-onset[]

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