Oct. 24, 2024 — A new mouse model mimicking the liver symptoms of myotonic dystrophy type 1 -- the most prevalent form of adult-onset muscular dystrophy -- provides insight into why patients ...
we propose that there are at least 4 clinically and genetically distinct forms of X-linked muscular dystrophy. IV-6 (A.C.), born in 1927, was not examined. He died of unrelated congenital heart ...
Since the isolation of the gene that causes Duchenne muscular dystrophy (DMD), scientists have progressed in understanding the mechanisms that lead to muscular diseases that can be evident from the ...
At the Breakthroughs in Muscular Dystrophy special meeting held in Chicago Nov. 19-20, 2024, and organized by the American Society of Gene & Cell Therapy (ASGCT), multiple interventions at the RNA ...
In addition, the infant exhibited pronounced muscular hypotonia (“floppy ... This strengthened the suspicion of congenital myotonic dystrophy type 1 (DM1) in the newborn. Autosomal dominant ...
U.S. News Live Presents: A Promising New Era in Treatment for Neuromuscular Diseases View video from this event: Neuromuscular diseases affect an estimated 41 out of every 100,000 young people ...
Carmela, from Devizes in Wiltshire, was diagnosed with the life-limiting condition LMNA Congenital MD at the ... of a marathon" for her. Muscular Dystrophy UK Carmela, along with her mother ...