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Increase awareness of the G2019S LRRK2 mutation in Parkinson's and no cost genetic testing program.
Full description
This program is intended to increase awareness of genetic Parkinson's, in particular the G2019S LRRK2 mutation, and provide no cost genetic testing to determine if they carry the G2019S LRRK2 mutation.
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Inclusion and exclusion criteria
Participants include those with a clinical diagnosis of Parkinson's, in particular those who have a first- or second-degree relative with Parkinson's, or who have young onset Parkinson's (age less than 50 at diagnosis) or are of Ashkenazi Jewish or North African Berber descent, or have a relative with a known genetic mutation in the LRRK2 gene, or who have a genetic mutation in the LRRK2 gene.
Inclusion Criteria:
Participant eligible for enrollment in the program must meet all of the following criteria:
Exclusion Criteria:
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Data sourced from clinicaltrials.gov
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