Why the study?
Should molecular screening be performed in family members of genotyped LQTS patients to identify silent gene carriers?
Population
Families with Long-QT Syndrome (LQTS)
Comparison
Molecular screening vs Clinical evaluation alone
Authors
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Clinical evaluation alone may miss silent LQTS carriers at risk; leaves open whether routine molecular screening improves family outcomes.
Should molecular screening be performed in family members of genotyped LQTS patients to identify silent gene carriers?
Clinical evaluation alone is insufficient to exclude LQTS in family members of affected patients; molecular screening is recommended to identify silent gene carriers.
Priori et al. (1999) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: