Clinical discoveries through collaborative research
Mayo Clinic is committed to advancing the understanding of the mechanisms of movement disorders, with clinical, lab, and genetic experts devoted to research that improves outcomes for patients. These efforts include searching for new biomarkers of disease as well as genetic causes, which, when confirmed, are added to our autoimmune and genetic test offerings. These same experts are available to help guide physicians in test ordering and results interpretation, lending their depth of experience in diagnosing and treating movement disorders to ordering physicians.
“As we learn more about these conditions, we are translating those advances into better testing for better patient care.”
The latest
Mayo Clinic Laboratories and Amprion, a global leader advancing diagnosis of neurodegenerative disorders through seed amplification testing, today announced a collaboration to expand access to Amprion's SAAmplify–αSYN (CSF) test across the United States. The test (test ID ASYNC) is available today for clients of Mayo Clinic Laboratories through the collaboration that combines the expertise of both organizations to enhance patient care and improve diagnostic accuracy for neurodegenerative diseases.
This “Specialty Testing” webinar will discuss the collaborative effort which led to the discovery of Kelch like protein 11 (KLHL11) IgG as a specific biomarker of neurological autoimmunity associated testicular germ cell tumor.
In this month’s “Hot Topic,” Andrew McKeon, M.B., B.Ch., M.D., reviews the use of neurological phenotype-based evaluations, the move away from the paraneoplastic evaluation, and upcoming changes to test profiles.
A movement disorder might be caused by the body’s immune system, which is meant to fight infections, suddenly attacking the brain. Fortunately, an “autoimmune movement disorder” can often be treated—once its cause is discovered.