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Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac condition and the most common cause of sudden cardiac death (SCD) in patients below the age of 35. Genetic testing is… Click to show full abstract
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac condition and the most common cause of sudden cardiac death (SCD) in patients below the age of 35. Genetic testing is a vital part of HCM diagnostics, yet correlation with clinical phenotypes remains complex. Identifying clinical predictors of informative genetic testing may prevent unnecessary investigations and improve cost‐effectiveness of services. This article reviews the current literature pertinent to identifying such predictors.
Keywords:
genotypes hypertrophic;
cardiomyopathy systematic;
clinical prediction;
systematic review;
hypertrophic cardiomyopathy;
prediction genotypes
Journal Title: European Journal of Clinical Investigation
Year Published: 2021
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Journal Title: European Journal of Clinical Investigation
Year Published: 2021
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!