Trial Information

Summary: Genetics of Dystonia

What is this research study about?

We use medical history information, family history information and genetic information to find genes that are associated with dystonia and to learn about what these genes do. We hope this research will determine what causes dystonia and how to develop new treatments.

What would I have to do?

First, you would talk with the research study staff about the research study and consent process. If you qualify to take part, we will ask you about your medical history, your family history and draw a family tree. Then you would give a blood sample.

All of this can be done at one appointment at Massachusetts General Hospital. If you live outside the Boston area, you can take part in the research study over the phone and through the mail.

What else do I need to know?

We get DNA from the blood sample. Your DNA is kept for many years. Research genetic test results are NOT given to people who take part in the research study. You will get no direct benefit from taking part in this research.


Eligibility Criteria:
Who can take part in the research study?

Anyone who is diagnosed with any type of dystonia, including:
•Generalized/Torsion
•Cervical/Spasmodic Torticollis
•Hand/Writer’s cramp
•Spasmodic dysphonia
•Belpharospasm

Family members 18 years old or older of people diagnosed with dystonia can also take part.

If you would like to learn more about participating in this study, please send an e-mail message using the form below.