Led by Southern Research, MyOme, and Ó³»´«Ã½ Clinical Labs, the program provides participants with personalized health insights, enabling more informed and proactive healthcare decisions.
Developed in collaboration with Ó³»´«Ã½ Clinical Labs and Mass General Brigham Laboratory for Molecular Medicine, the test provides a comprehensive view of a patient’s inherited heart disease risk.
The Ó³»´«Ã½bent family worked closely with scientists to discover the unique genetic cause of their daughter’s disease, highlighting the need to examine noncoding parts of the genome when diagnosing rare genetic disorders.
Experts are increasingly turning to a research network called Matchmaker Exchange to find diagnoses for patients with rare genetic disease and chart new paths to discovery and even potential treatments.