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  2. Parkinson's disease - Wikipedia

    en.wikipedia.org/wiki/Parkinson's_disease

    Parkinson's typically manifests in individuals over 60, with about one percent affected. In those younger than 50, it is termed "early-onset PD". No cure for Parkinson's is known, and treatment focuses on alleviating symptoms. Initial treatment typically includes L-DOPA, MAO-B inhibitors, or dopamine agonists.

  3. Too young for Parkinson’s? What it’s like being diagnosed in ...

    www.aol.com/news/too-young-parkinson-being...

    Ahead of World Parkinson’s Day on April 11, Abi Jackson talks to two people living with early-onset symptoms. Skip to main content. 24/7 Help. For premium support please call: 800-290-4726 more ...

  4. Signs and symptoms of Parkinson's disease - Wikipedia

    en.wikipedia.org/wiki/Signs_and_symptoms_of...

    Parkinson's disease patient showing a typical flexed walking posture in advanced stage. Signs and symptoms of Parkinson's disease are varied. Parkinson's disease affects movement, producing motor symptoms. [1] Non-motor symptoms, which include dysautonomia, cognitive and neurobehavioral problems, and sensory and sleep difficulties, are also ...

  5. Can your smartwatch detect if you have early Parkinson ... - AOL

    www.aol.com/smartwatch-detect-early-parkinson...

    New research reports that everyday smartwatches and smartphones could potentially be used to measure changes in Parkinson's symptoms over time in people in the early stages of the disease.

  6. Hope for Parkinson’s disease symptoms is found in ... - AOL

    www.aol.com/finance/hope-parkinson-disease...

    Tavapadon, a drug being tested to treat early Parkinson's disease, has shown great promise in a Phase III trial by AbbVie, the pharmaceutical company announced this week.. Parkinson’s disease ...

  7. Kufor–Rakeb syndrome - Wikipedia

    en.wikipedia.org/wiki/Kufor–Rakeb_syndrome

    Kufor–Rakeb syndrome is associated with mutations in the ATP13A2 gene. [8] The inheritance pattern for KRS is autosomal recessive. [9] If a male and female carrier, who each have one mutation in ATP13A2 have a child, there is a 25% chance the child has KRS, a 50% chance the child is a carrier for KRS, and a 25% chance the child does not have KRS.