Myotone Dystrophie Typ 1

Myotonic dystrophy refers to a group of progressive multi-system genetic disorders that affect primarily muscle function, but can also affect other organs such as the heart, eye and endocrine system.

There are currently two clinically and molecularly defined forms of myotonic dystrophy:

• myotonic dystrophy type 1 (DM1) (Steinert disease)
• myotonic dystrophy type 2 (DM2) (proximal myotonic myopathy) 

Epidemiology

The estimated incidence is ~1:8,000 individuals.

See also 

• muscular dystrophy

Siehe auch:

• Muskeldystrophie
• Myotonia congenita
• Myotone Dystrophie Typ 2
• Myotonia congenita Thomsen