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J Am Podiatr Med Assoc · Jul 1998
Review Case Reports Comparative StudyContrasts in clinical presentation and genetic transmission of myotonic dystrophy.
- H Reifer and E Sobel.
- Department of Orthopedics, New York College of Podiatric Medicine, New York 10035, USA.
- J Am Podiatr Med Assoc. 1998 Jul 1;88(7):313-22.
AbstractMyotonic dystrophy, the most common inherited neuromuscular disease, is an autosomal dominant muscular dystrophy characterized by myotonia and distal muscle weakness. It is caused by an increase in the number of cytosine-thymine-guanine (CTG) nucleotide repeats present on the long arm of chromosome 19. Two patients were evaluated, one with classic adult-onset myotonic dystrophy and the other with congenital myotonic dystrophy. Contrasts in the clinical features and genetic transmission of this disease and clinical management are reviewed.
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