Genetic Screening Outcomes in Movement Disorders

Brief description of study

Understanding the correlation between genetic mutations and causative pathogenic mechanisms and phenotypes in Movement Disorders may significantly contribute to implementing therapeutic approaches for these conditions. With the present study we aim to assess the rate of positivity of genetic testing in a cohort of patients with Movement Disorders. This study will provide valid information to improve genetic counseling to our patients, to help stratifications of cases (which is crucial for clinical trials), and to guide decision for genetic tests in the future.

Clinical Study Identifier: s21-01120

Principal Investigator: Giulietta Maria Riboldi.

Other Investigator: Steven J. Frucht.

Contact the research team to learn more about this study.

Your Email

Not a valid e-mail address

Please Provide Email Address

First Name

First name is mandatory

Last Name

Your Phone

Please provide phone number

Invalid phone number

Valid phone number

Comments

Send Confirmation of This To Me

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.

Clinical Research Studies