This site focuses on medical research (i.e. advances) that have been made in the field of cardiovascular genetics, as well as information on different types of genetic heart-related diseases and cardiac genetic testing that occurs in order to determine which cardiac condition the patient is suffering from. Cardiac genetic conditions are those that children inherit at birth from their parents. There are various treatments (insurance covered as well as Medicaid and/or Medicare covered) for genetic heart-related diseases available today due to breakthroughs in the field of Cardiology, and we cover them all!
A Few Things to Know
Medical conditions that run in a family are often inherited, whether from the parent or grandparent, in the form of genetic mutations. Gene mutations can carry with them some of the most dangerous diseases known to humanity, one such lethal disease is heart disease. There are different types of heart-related conditions that can be inherited. Conditions such as high blood pressure, high cholesterol, diabetes, and coronary artery disease — just to name a few — run in families. There is no single genetic change that results in serious heart conditions, but, rather, a multitude of genetic changes. heart conditions do not result from a single genetic change, but result from a multitude of genetic changes that work collectively to cause the disease. In these situations, genetic testing is not yet available. However, there are other inherited heart diseases that are caused by either one or very few genetic changes. Singular genetic changes, such as these, are called monogenic conditions and genetic testing is available for these conditions.
How Does Inheritance Work?
Genes are the basic units of inheritance and are made up of molecules called DNA. Genes provide instructions for cells to make proteins that carry out all of our body’s functions and form our physical characteristics. Most genetic heart conditions are inherited in an autosomal dominant pattern — effecting both men and women equally. The autosomal mutation need just exist in one gene in order for it to take on a dominant role in transferring from parent to child at a rate of 50%. The child, in turn, also has a 50% chance of passing the same autosomal mutation to his/ her children — also at a rate of 50% — and the cycle continues.