Progeria Syndrome

Progeria Syndrome

Huntington's disease

Huntington's disease

Color Blindness

Color Blindness

Wednesday, April 21, 2010

Huntington's disease

Huntington's disease is a disorder passed down through families in which certain nerve cells in the brain waste away. There are two forms of Huntington's disease. The most common is adult-onset Huntington's disease. Persons with this form usually develop symptoms in their mid 30s and 40s.
An early-onset form of Huntington's disease accounts for a small number of cases and begins in childhood or adolescence. Symptoms may resemble those of Parkinson's disease with rigidity, slow movements, and tremor.




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