Parkinson disease 2, autosomal recessive juvenile (PARK2): Type 2 Parkinson disease is juvenile form of the condition and is linked to a genetic mutation on chromosome 6q25.2-q27. The condition may be inherited in a recessive manner and symptoms tend to be milder following sleep. Parkinson's disease is a chronic, progressive, degenerative brain disorder characterized by tremors, muscle rigidity and slowed movements. More detailed information about the symptoms, causes, and treatments of Parkinson disease 2, autosomal recessive juvenile (PARK2) is available below.
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Prognosis for Parkinson disease 2, autosomal recessive juvenile (PARK2): There is no cure for the condition and the rate of progression varies amongst patients. Various therapies can reduce the impact of symptoms and allow a better quality of life.
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