Friedreich's ataxia is a rare disease passed down through families (inherited) that affects the muscles and heart.
Spinocerebellar degeneration
Friedreich's ataxia is caused by a defect in a gene called Frataxin (FXN), which is located on chromosome 9. Changes in this gene cause the body to produce too much of part of DNA called trinucleotide repeat (GAA). Normally, the body contains about 8 to 30 copies of GAA....
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Source: ADAM Encyclopedia
Ataxia-telangiectasia is rare childhood disease that affects the brain and other parts of the body.Ataxia refers to uncoordinated movements, such as... Read more »
Source: HealthCentral Encyclopedia
Ataxia is defined as the failure of muscle coordination that generally results in an unsteady gait and balance, limb or eye movements, and/or... Read more »
Ataxia: and unsteadiness due to the brain’s failure to regulate the body’s posture and regulate the strength and direction of limb movements.... Read more »
Source: ADAM Encyclopedia
Acute cerebellar ataxia is sudden onset of uncoordinated muscle movement. Alternative Names Cerebellar ataxia; Ataxia - acute... Read more »