Myotonic dystrophy - Wikipedia - myotonic adult muscular dystrophy


Myotonic muscular dystrophy, Myotonic Dystrophy Type 1, Myotonic Dystrophy Type 2 myotonic adult muscular dystrophy

The CTG repeat size in adult onset is generally in the range of 50 to 1, The mild form of DM1 is characterized by mild weakness, myotonia, and cataracts.

Myotonic dystrophy (DM) is a form of muscular dystrophy that affects muscles and are some of the most common forms of adult-onset muscular dystrophy.

Myotonic dystrophy (DM) is a genetic disorder characterized by both progressive Adults with DM1 may experience symptoms of muscle wasting and muscle.

Myotonic dystrophy is part of a group of inherited disorders called muscular dystrophies. It is the most common form of muscular dystrophy that.

Myotonic dystrophy refers to two rare genetic disorders of muscle that actually affect . People with the classic or adult form of DM are also at a greater risk of.