There are currently 2 forms of Myotonic Dystrophy: Type 1 Myotonic Dystrophy (Steinert Disease) and Type 2 Myotonic Dystrophy.

 Myotonic (Steinert’s disease): The myotonic form is the most common adult-onset form.

Myotonic (Steinert’s disease): The myotonic form is the most common adult-onset form.

The work described herein also makes available a DM transcription unit or gene which is likely to have an important role in the pathophysiology of DM.

Myotonic (Steinert's disease): The myotonic form is the most common adult-onset form.

Type 2, also known as proximal myotonic myopathy (PROMM) – is caused by a mutation in the CNBP gene.

In 1994, a particular form of Myotonic Dystrophy with a different genetic anomaly than classic Myotonic Dystrophy (DM1) was described.

a degenerative muscular disorder, myotonic dystrophy (MD); and

Methods of treating myotonic dystrophy using the chimeric polypeptide.

Myotonic (also called MMD or Steinert’s disease)

· Myotonic (also called MMD or Steinert's disease).

The present invention relates to a method for diagnosing myotonic dystrophy type 1 or a method for identifying myotonic dystrophy type 1 patients by using a computer processor.

dystrophy of the myotonic type (underdevelopment of muscles),

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Frequency of damage to the nerves in myotonic dystrophy.