A recent discovery of a molecular connection between autism and myotonic dystrophy, a type of neuromuscular disease, may provide a breakthrough on how clinicians approach autism spectrum disorder.

Use precise geolocation data and actively scan device characteristics for identification. This is done to store and access ...

Mar. 3, 2025 — Researchers have shown how a low carbohydrate diet can worsen the DNA-damaging effects of some gut microbes to cause colorectal cancer. The study compared the effects of three ...

After a primary care visit, columnist Robin Stemple faces a battery of tests and appointments, which he calls a medical merry ...

Biophytis SA (FP: ALBPS), ("Biophytis" or the "Company"), a clinical-stage biotechnology company specializing in the development ...

Here are the causes and treatment for the congenital disorder Duchenne muscular dystrophy! Entering the age of 2 years, almost most children will start to actively explore their surroundings. However, ...

About Myotonic Dystrophy Type 1 Myotonic dystrophy type ... The disease is highly variable with respect to severity, presentation and age of onset, however all forms of DM1 are associated with ...

Upon approval, vamorolone would be the first and only treatment option indicated for patients diagnosed with Duchenne muscular dystrophy in Canada The Canadian regulatory submission of vamorolone ...

More information: Dariusz C. Górecki et al, Is dystrophin immunogenicity a barrier to advancing gene therapy for Duchenne muscular dystrophy? Gene Therapy (2025). DOI: 10.1038/s41434-025-00531-y ...

About the Phase 3 HARBOR™ Trial Myotonic dystrophy type 1 (DM1) is an underrecognized ... The disease is highly variable with respect to severity, presentation and age of onset, however all forms of ...

Suneel Ram’s needs gradually became greater after he was diagnosed at age 3 with Duchenne muscular dystrophy, a muscle-wasting genetic disorder that afflicts one in 5,000 boys. Today ...