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Results 1 - 8 of 8 for Spinocerebellar "ataxia," autosomal recessive 8
  1. ... Related Autosomal Recessive Cerebellar Ataxia Genetic Testing Registry: Spinocerebellar ataxia, autosomal recessive 8 Johns Hopkins Medicine Department of Neurology and Neurosurgery: ...
  2. 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, ... autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS); and ...
  3. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Spinocerebellar ataxia 23(SCA23) Spinocerebellar ataxia 24(SCA24); SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4 Spinocerebellar ataxia 25(SCA25) Spinocerebellar ataxia ...
  4. Cerebellar Disorders (National Library of Medicine)  
    When you play the piano or hit a tennis ball you are activating the cerebellum. The cerebellum is the area of the brain that controls coordination and balance. ...
  5. ... trinucleotide repeat (GAA). Normally, the body contains about 8 ... autosomal recessive genetic disorder. This means you must get a ...
  6. Friedreich's Ataxia (FA) (Muscular Dystrophy Association) - PDF  
    ... to straighten and stabilize the spine. rod screw ... is inherited in an autosomal recessive pattern. Autosomal refers to the fact that the ...
  7. Classification of Ataxia (National Ataxia Foundation)  
    ... SCA7 – Spinocerebellar Ataxia Type 7 Dominant Yes SCA8 – Spinocerebellar Ataxia Type 8 Dominant Yes SCA10 – Spinocerebellar Ataxia Type 10 Dominant ... Type 1 and Type 2 Recessive Yes ARSACS -Autosomal Recessive Ataxia of Recessive Yes Charlevoix-Saguenay AVED -Ataxia, ...
  8. Genetics Home Reference: Friedreich ataxia From the National Institutes of Health (National Library of Medicine)  
    ... Friedreich ataxia? This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...