Myotonic dystrophy, type 2 |
DM2; PDM; PROMM; Proximal myotonic dystrophy; Proximal myotonic myopathy; Ricker syndrome |
Myotonic dystrophy, type 2 is an inherited disorder of the muscles and other body systems. Type 2 myotonic dystrophy tends to be milder than type 1, and the two forms are caused by mutations in different genes. Myotonic dystrophy, type 2 is a subtype of myotonic dystrophy. Many of the signs and symptoms seen with this disorder are similar to those of type 1 myotonic dystrophy, including progressive muscle weakness, prolonged muscle contractions (myotonia), clouding of the lens of the eye (cataracts), cardiac abnormalities, balding, and infertility. The clinical features of type 2 vary widely among people, however, and tend to be milder than those seen with type 1 myotonic dystrophy. Congenital myotonic dystrophy (a form of the disorder that is evident from birth) has not been seen in families with type 2.
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Myotonic dystrophy, type 2 Other1 of 1
Myotonic dystrophy, type 2
... Myotonic dystrophy, type 2 is an inherited disorder of the muscles and other body systems. Type 2 myotonic dystrophy tends to be milder than type 1, and the two forms are caused by mutations in differ...
Source: Genetics Home Reference
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Myotonic dystrophy, type 2 Articles
- Myotonic dystrophy, type 2
... Myotonic dystrophy, type 2 is an inherited disorder of the muscles and other body systems. Type 2 myotonic dystrophy tends to be milder than type 1, and the two forms are caused by mutations in differ...

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