Focus On: DYT1 Dystonia

DYT1 dystonia, also known as early-onset torsion dystonia, is a severe form of hereditary, generalized dystonia.

Journeys into Parenthood

This article was published in the Dystonia Dialogue. The path to becoming a parent for individuals in the dystonia community is as varied as society at large. There are more options than ever for having children: biologically, via reproductive medicine, fostering, and adoption. Parents with dystonia may encounter challenges that parents without health issues might […]

Dystonia Genes Converge in Specific Neurons & Intersect Underlying Genetic Basis of Psychiatric Disorders

There are many types of dystonia, often presenting with very distinct symptoms. There is also a great deal of overlap in the physical manifestation of symptoms across the different types. Non-motor symptoms are common, including psychiatric disorders such as depression and anxiety. There have been numerous genes identified to cause dystonia, and it is not […]

DMRF Research Grants Fund Diverse Investigations into Dystonia Origins

Dystonia is a movement disorder characterized by excessive muscle contractions that cause abnormal movements and postures. Dystonia is not caused by pathology in a specific brain structure, but by dysfunctional circuits of communication between multiple brain areas responsible for coordinating and controlling body movement. Despite substantial progress made in understanding various aspects of dystonia, there […]

40+ Years of DMRF Research Achievements

“DMRF initiated, supported, stimulated, and catalyzed essential scientific and medical efforts that created the modern dystonia field.” -Jan Teller, MA, PhD Chief Scientific Advisor Nearly 45 years ago, the DMRF began the ambitious mission to find a dystonia cure. Since that time, the Foundation has provided funding to 270+ investigators and has grown the field […]