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They are both inherited as autosomal dominant trait, differing only by the characteristic of DM2 that contains one or more ion-channel defects. The second type of myotonic dystrophy is rarely found; therefore I will focus my research mainly on type 1. Here, clinical findings have been categorized into three phenotypes: congenital, classical, and mild. In congenital MMD, onset occurs in infancy or early childhood of less then 10 years of age. During infancy, the disease may be characterized by hyponia with sucking and swallowing, and severe generalized weakness at birth, often with respiratory deficiency and early death...
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