This is a longitudinal study in patients with Parkinson's Disease (PD) carriers of a genetic mutation - substitution of gly with ser in position 2019 (G2019S) in the leucine-rich repeat kinase 2 (LRRK2) gene. The purpose of this study is to explore the association between genetic mutations in the known genes and their influence on disease manifestation over few years of follow up
Study Type
OBSERVATIONAL
Enrollment
200
motor and cognitive functions
Tel Aviv Sourasky Medical Center
Tel Aviv, Israel
change from baseline in updrs motor and total scores
Time frame: the participants will be followed for 5 years. the measurements will be taken evry 18 month.
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