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Article

Myotonic dystrophy type 2.

European journal of neurology - 1 Sept 2002

Finsterer J

Abstract excerpt

Myotonic dystrophy type 2 (DM2) is a clinically but not genetically heterogeneous, multisystem disorder, that is clinically similar to, but distinct from myotonic dystrophy type 1 (DM1). Initially, different phenotypes of DM2 were described by Ricker (proximal myotonic myopathy, PROMM), Ranum (myotonic dystrophy 2, DM2) and Udd (proximal myotonic dystrophy, PDM). Clinical features these three phenotypes had in...

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Identifiers

PMID: 12220374
DOI: 10.1046/j.1468-1331.2002.00453.x

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