Short QT syndrome risk factors: Difference between revisions
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Created page with "__NOTOC__ {{Short QT syndrome}} {{CMG}} ==Overview== Short QT syndrome is an autosomal dominantly inherited disease, and having a family member with the disase places an indi..." |
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==Overview== | ==Overview== | ||
Short QT syndrome is an autosomal | Short QT syndrome is an autosomal dominant inherited disease, and having a family member with the disase places an individual at risk for the disease. Family members of affected individuals should therefore be screened. New onset [[lone atrial fibrillation]] may be a marker of the disease, and young patients with [[lone atrial fibrillation]] should be screened as well. | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Latest revision as of 18:04, 3 September 2012
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Short QT syndrome risk factors On the Web |
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Risk calculators and risk factors for Short QT syndrome risk factors |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Short QT syndrome is an autosomal dominant inherited disease, and having a family member with the disase places an individual at risk for the disease. Family members of affected individuals should therefore be screened. New onset lone atrial fibrillation may be a marker of the disease, and young patients with lone atrial fibrillation should be screened as well.