Parkinson disease 6, autosomal recessive early-onset (PARK6): Type 6 Parkinson disease is an early-onset form of the condition and is linked to a genetic mutation on the PINK1 gene on chromosome 1p36. The condition may be inherited in a recessive manner and symptoms tend to fluctuate during the day. 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 6, autosomal recessive early-onset (PARK6) is available below.
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Prognosis for Parkinson disease 6, autosomal recessive early-onset (PARK6): 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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