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Ann Neurol ; 70(4): 662-5, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22028225

ABSTRACT

The prevalence of congenital myopathies in the United States has not been examined. To address this, we determined the point prevalence of congenital myopathies in a well-defined pediatric population from Southeastern Michigan. The overall point prevalence was 1:26,000. Mutations in RYR1 were the most common cause of congenital myopathies at 1:90,000. Our data broadly agrees with estimates from previous European studies and provides the first estimate of the prevalence of congenital myopathies in the United States. Ann Neurol 2011;70:662-665.


Subject(s)
Muscular Dystrophies/epidemiology , Muscular Dystrophies/genetics , Ryanodine Receptor Calcium Release Channel/genetics , Child , Female , Humans , Male , Michigan/epidemiology , Mutation , Prevalence , United States/epidemiology
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