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Results 1 - 7 of 7 for Spinocerebellar ataxia 17
  1. ... Registry: Huntington disease-like 3 Genetic Testing Registry: Spinocerebellar ataxia 17 You might also find information on the diagnosis ...
  2. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Spinocerebellar ataxia 15(SCA15) Spinocerebellar ataxia 16(SCA16) Spinocerebellar ataxia 17(SCA17) Spinocerebellar ataxia 18(SCA18) Spinocerebellar ataxia 19( ...
  3. Classification of Ataxia (National Ataxia Foundation)  
    ... SCA16 – Spinocerebellar Ataxia Type 16 Dominant No SCA17 – Spinocerebellar Ataxia Type 17 Dominant Yes SCA18 – Spinocerebellar Ataxia Type 18 Dominant No SCA19 – Spinocerebellar Ataxia Type ...
  4. Gene Testing for Hereditary Ataxia (National Ataxia Foundation) - PDF  
    ... As of 2013, genetic testing is available for spinocerebellar ataxia types 1, 2, 3, 5, 6, 7, 8, 10, 12, 13, 14, 17, 28; dentatorubropallidoluysian atrophy (DRPLA); ataxia-telangiectasia (A-T); ...
  5. Sporadic Ataxia and Multiple System Atrophy (MSA) (National Ataxia Foundation) - PDF  
    ... diagnosis of dominantly inherited ataxia, (which is called spinocerebellar ... 3, 5, 6, 7, 8, 10, 12, 13, 14, 17 and 28. Genetic testing also is available for ...
  6. Muscular Dystrophy: Hope Through Research From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... 15 other disorders, including Huntington's disease and the spinocerebellar ataxias. Oculopharyngeal MD (OPMD) generally begins in a person's ...
  7. National Institute of Neurological Disorders and Stroke (National Institute of Neurological Disorders and Stroke)  
    ... the BRAIN Initiative in fiscal 2014 , Tuesday, December 17, 2013 NINDS News Feed » More News » Follow NINDSnews » ... Sclerosis Prion Diseases Progressive Hemifacial Atrophy Progressive Locomotor ... Atrophy Spinocerebellar Degeneration Steele-Richardson-Olszewski Syndrome Stiff- ...