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Results 1 - 10 of 17 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. 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); ...
  4. 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 ...
  5. ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Spinocerebellar ataxia type 1 (often shortened to SCA1 ) On this ... Glossary definitions Reviewed February 2011 What is SCA1? Spinocerebellar ataxia type 1 (SCA1) is a condition characterized by ...
  6. ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Spinocerebellar ataxia type 6 (often shortened to SCA6 ) On this ... Glossary definitions Reviewed February 2011 What is SCA6? Spinocerebellar ataxia type 6 (SCA6) is a condition characterized by ...
  7. ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Spinocerebellar ataxia type 2 (often shortened to SCA2 ) On this ... Glossary definitions Reviewed February 2011 What is SCA2? Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by ...
  8. ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > Spinocerebellar ataxia type 3 (often shortened to SCA3 ) On this ... Glossary definitions Reviewed February 2011 What is SCA3? Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by ...
  9. ... literature OMIM Genetic disorder catalog Conditions > Infantile-onset spinocerebellar ataxia (often shortened to IOSCA ) On this page: Description ... Reviewed March 2010 What is IOSCA? Infantile-onset spinocerebellar ataxia (IOSCA) is a progressive disorder that affects the ...
  10. ... Related Autosomal Recessive Cerebellar Ataxia Genetic Testing Registry: Spinocerebellar ataxia, autosomal recessive 8 Johns Hopkins Medicine Department of ...
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