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Key terms: form repeat type patients symptoms dm muscle severe genetic medical myotonic dystrophy disorder chromosome disease onset diagnosis research defect larger weakness problems exist presentation expansion milder myotonia treatment protein pattern splicing proximal clinical affected multiple specific hypersomnia anticipation phenotype inherited molecular screening cataracts cognitive neuromuscular conduction sleepiness muscular dystrophy abnormalities trinucleotide repeat disorder Search external links cited by footnotes on Wikipedia page Myotonic dystrophy: |
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