This strengthened the suspicion of congenital myotonic dystrophy type 1 (DM1) in the newborn. Autosomal dominant congenital DM1 is due to a CTG repeat expansion of the DMPK (dystrophia myotonica ...
Click here to learn more from DelveInsight’s latest report @ Myotonic Dystrophy Market Size AMO-02 (tideglusib) is under development for congenital myotonic dystrophy (CDM) and potential use in ...
Description: There are various forms of Muscular Dystrophy, including Becker, Congenital, Duchenne, Distal, Emery-Dreifuss, Facioscapulohumeral, Limb-Girdle, Myotonic ...
People with Myotonic Dystrophy Type 1 (DM1), the most common adult-onset form of muscular dystrophy, progressively lose muscle mass and strength in their lower legs, hands, neck and face.
People with myotonic dystrophy type 1 (DM1), the most common adult-onset form of muscular dystrophy, progressively lose muscle mass and strength in their lower legs, hands, neck and face.
Myotonic dystrophy type 1 (DM1 ... during adulthood (classic DM1), although DM1 can develop at birth in a congenital form, or during childhood. Although signs and symptoms vary among affected ...