Towards a treatment for myotonic dystrophy: First 3D model with patient cells. Myotonic dystrophy is a hereditary degenerative neuromuscular disease that occurs mainly in adults, affecting about ...

DelveInsight’s 'Myotonic Dystrophy Pipeline Insight – 2023' report provides comprehensive global coverage of available, marketed, and pipeline myotonic dystrophy therapies in various stages of ...

In myotonic dystrophy, like the other types of MD, faulty DNA is to blame for the abnormalities that occur. Weakness. Myotonic dystrophy occurs because of a large expansion of DNA code, which most ...

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.

DESPITE the frequent occurrence of ventilatory insufficiency and congestive heart failure in myotonic and progressive muscular dystrophy,1 2 3 the cardiac and pulmonary disturbances in these disord ...

Correction of Clcn1 alternative splicing reverses muscle fiber type transition in mice with myotonic dystrophy. Nature Communications , 2023; 14 (1) DOI: 10.1038/s41467-023-37619-1 Cite This Page : ...

JUV-161 is a first-in-class muscle regenerating biologic that will address myopathies starting with Myotonic Dystrophy Type 1 ; JUV-161 was discovered using Juvena’s proprietary JuvNET platform ...

Myotonic Dystrophy Type 1 (DM1) is the most common adult-onset form of muscular dystrophy and a condition that severely affects multiple organs including skeletal muscle, heart, brain and the ...