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Myotonic Dystrophy Cmyd

What is Myotonic Dystrophy? Myotonic Dystrophy (DM) is an inherited disorder. It is abbreviated as Congenital Myotonic Dystrophy (CMyD).

Myotonic Dystrophy Cmyd is described in multiple online sources, as addition to our editors' articles, see section below for printable documents, Myotonic Dystrophy Cmyd books and related discussion.

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Myotonic Dystrophy April10
Congenital Myotonic Dystrophy (CMyD). DM affects both males and females. Age of onset is variable from birth through to old age.
Myotonic Dystrophy
Myotonic Dystrophy is caused by an expansion of part of the chromosomes, either Chromosome 19 for DM1 and CMyD, or Chromosome 3 for DM2.
Mitochondrial DNA does not appear to dystrophy
of congenital myotonic dystrophy (CMyD) re- main unexplained.
Lower gastrointestinal tract disturbance in congenital myotonic
Congenital myotonic dystrophy (CMyD) is an aut- osomal dominantly inherited, multi-system disorder, characterised by myotonia, atrophy, and weakness.
Employees with Muscular Dystrophy Accommodation and
Myotonic Dystrophy (CMyD), both forms of muscular dystrophy.

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Sections MENTAL RETARDATION What does this term mean
The congenital variant of Myotonic Dystrophy (CMyD) is transmitted by the affected mothers to children with the CMyD gene, in the region q13.
Myotonic Dystrophy
Myotonic dystrophy - a knol by Manuel Menendez
Myotonic Dystrophy April10
Congenital Myotonic Dystrophy (CMyD). DM affects both males and females. Age of onset is variable from birth through to old age.
Congenital myotonic dystrophy associated with a chromosome
We report two cases of congenital myotonic dystrophy (CMyD) associated with a chromosome abnormality of pericentric inversion.

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