An inherited heart condition is a problem with the heart that runs in families. This means it's passed down through your genes from your parents. These conditions can affect the heart's structure or how well it works. Here are three main types:
Because certain heart disorders are hereditary, you may think that genetic testing holds the key to diagnosis and treatment. In most cases, however, that's not how it works.
The most important piece of the diagnostic puzzle may lie in your family history. Ask your parents, grandparents, brothers, and sisters about any health problems, then tell your doctor about conditions that show up in multiple family members. You don't need to go back too far; focus on recent generations, as older medical records and lifestyles were very different.
Your doctor will use a combination of your family medical history and modern diagnostic tools to determine whether you have an inherited heart condition. Genetic heart rhythm disorders are diagnosed using an electrocardiogram (ECG or EKG) test—which checks your heart's electrical signals—and inherited cardiomyopathies may be diagnosed using minimally invasive methods such as echocardiogram or cardiac catheterization to view the structure of the organ. If high cholesterol runs in your family and doesn’t improve with lifestyle changes like diet and exercise, it’s likely hereditary and may not need further testing.
Some genetic heart problems can be very serious, even causing sudden death. That's why early diagnosis is so important. If your family exhibits a history of heart problems, be sure to provide your doctor (and your children's pediatrician) with a solid family history. When these inherited heart conditions are found early, they can often be treated or watched closely. These early interventions may help you live a long, healthy life, no matter what your DNA says.
Copyrighted material adapted with permission from Ignite Healthwise, LLC. This information does not replace the advice of a doctor.
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