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Article

Clinical and genetic heterogeneity in myotonic dystrophies

1 Jan 2000

Abstract excerpt

This review of myotonic dystrophies primarily concentrates on the clinical and genetic findings that can distinguish a novel form of myotonic dystrophy, myotonic dystrophy type 2 (DM2); proximal myotonic myopathy (PROMM); and proximal myotonic dystrophy (PDM) from myotonic dystrophy type 1 (DM1). The multisystemic nature of these disorders leads to a spectrum of symptoms and signs. Careful clinical evaluation of...

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Identifiers

PMID: 11102902
DOI: 10.1002/1097-4598(200012)23:12<1789::aid-mus2>3.0.co;2-4

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