EDS research

Research Round-up, Edition Six

Previous editions of Research Round-up can be found at the following links: Edition 5 (Pediatrics)   Edition 4 (Neurodivergence)   Edition 3   Edition 2   Edition 1 Howdy, partners! This Research Round-up has roped in a whole herd of topics for you. We hope you enjoy the read, learn a thing or two, and feel […]

Digital graphic with a dark blue DNA helix and bold text reading ‘Update on gene linked to hypermobile EDS’ on a light blue background

Update On Gene Linked to Hypermobile EDS

A new study, led by Dr. Cortney Gensemer, marks a genetic breakthrough in hEDS research. The KLK15 variant (p.Gly226Asp) has been identified as a direct disease-causing gene in hypermobile EDS, causing connective tissue dysfunction and immune system dysregulation.