Genetic Testing For Heart Disease
What is genetic testing for heart disease? Genetic testing involves checking the blood of a person, his tissues, organs, or other body fluids to determine whether genetic abnormalities may underlie any underlying medical conditions. Testing can also be used to diagnose or screen for other diseases. Some tests may also use antibodies to identify abnormal proteins within the blood.
Genetic testing is becoming more common and is performed on people of all ages. There are many types of genetic tests and the results are reported to the family. It is an excellent way to find out if someone in the family has inherited a health problem, such as certain types of cancer or heart disease, from their parents or grandparents.
Genetic Testing for heart disease can be as simple as a cheek swab or can be a very complex process
When genetic testing is done, the geneticists will run tests on the affected person. The doctor will collect and store samples from the person and take the sample to an accredited laboratory for analysis. The results can indicate whether there is a family history of certain medical conditions, such as heart disease. If the results show that the genetic problem was inherited, then the family may be able to take precautions against future problems. The results can also help to identify any abnormalities that could develop into heart disease or certain types of cancer.
Genetic testing can be a complex process. There are many different types of tests used in this process. Genetic testing can be done by the patient or by the doctor. It is usually done on a person at the same time he is tested for a medical condition. In this way, the results can be compared with results obtained after the tests have been conducted.
Do You Or Any Of Your Family Members, (Children, Grandchildren, Parents, Siblings) Have Any Of The Following Problems?
Have heart disease, a pacemaker, or has someone in your family had heart disease?
Have Cancer or has someone in your family had cancer?
Have problems with prescription drug interactions?
Have problems with prescription drug interactions?
Regularly take 3 or more prescription drugs?
Have any other medical problem you may worry about?
Then you should take our No Cost / No Obligation simple 4 question survey to see if you possibly qualify for genetic testing.
Remember, what you learn could possibly save you or one of your family member’s lives! Take 3 minutes and do the survey. It is No Cost and No Obligation, BUT it could possibly make a lifetime of difference!
Possible tests a doctor may perform if they suspect your baby may have heart disease when it is born
There are two ways that medical tests are done, and these can be done at the same time. If the doctor suspects that a test result may indicate a serious health concern, then a procedure called a prenatal genetic screening may be performed. Prenatal genetic screening is used in order to determine if the baby is at risk for certain medical conditions such as congenital heart disease, and other genetic defects that could lead to serious diseases and premature death.
Another type of procedure is called physical examination and is used when a doctor suspects that a genetic abnormality could be present. The physical examination includes a complete medical and family history of the person along with blood work, laboratory tests and x-rays.
Protein tests are also done during this process. Protein tests are used to determine the levels of specific proteins in the blood that are known to be associated with the development of various medical conditions and are related to a particular disease.
Genetic Testing can help your doctor make an informed decision as to how to treat you or a family member
Genetic testing can provide results to help doctors make an informed decision about treatment. Often, it will help determine the extent of the disease and its severity and even how to prevent its recurrence.
Before the procedure is performed, the health care provider will perform a thorough medical and family history to determine if a problem exists. The patient’s health history will be reviewed to determine if he is a good candidate for the procedure. Also, the patient will be screened for other medical conditions and symptoms in order to help determine which procedure is appropriate for him.
After all of these checks and examinations, the genetic counselor can determine whether or not the test is necessary. He will discuss the procedure with the patient and will determine if he can be helped with the procedure.
For patients who are uninsured or have limited health insurance coverage, the procedure may not be covered. The patient can arrange with his or her insurance provider if he or she would like to receive the procedure through a co-pay program.
In cases where the procedure is covered by the health care provider, they will explain the procedure to the patient and make sure that the patient understands what is required. When the procedure is covered, the patient may receive a written estimate for the co-pay amount.