Genetic Heart Problems
A View Of Genetic Heart Problems
One of the most dreaded illnesses anyone could have are genetic heart problems, and this is for good reason. There is very little one can do to prevent the onset of a genetic heart condition. Even adopting an extremely healthy lifestyle can only serve to lower the risks but not necessarily cure or eliminate the disease. For the most part, anyone with genetic heart problems will always be pre-disposed to feeling the effects of the disease at one point or another. Whether these symptoms get worse or not, however, is an altogether different story.
For this reason, it is extremely important to spot medical symptoms and conditions that could lead to potential early diagnosis of genetic heart problems. Especially if a family has been definitively ruled to have genetic tendencies for heart ailments, knowing that the risks are higher for a specific family tree can encourage an individual to change their living habits to try to minimize their risks as much as possible.
Here are things one should watch out for as potential early signs of genetic heart problems:
Heart failure for any immediate and close family member at ages below 50. This typically indicates an increased propensity for the disease as non-genetic heart failure cases usually only occur at age 70 and above.
Blackouts, seizures, or fainting that cannot be diagnosed or treated with ordinary seizure treatment methods.
Unexplainable asthma-like shortness of breathing that is not remedied by asthma medication or inhalers.
If there is more than one close relative that has the same heart illness, then the condition is most likely genetic.
Unexplained fatalities in the family can normally be traced to stroke or cardiac arrest. This emphasizes the importance of securing an autopsy or at least a medical diagnosis of the actual cause of death and to not be complacent with incidents without understanding why they happen.
Abnormal heartbeat sometimes falsely diagnosed as simple transient idiopathic arrhythmia when it can be the symptom of something else more serious.
It is difficult to enumerate all potential forms of genetic heart problems because of the sheer length of the list. However, it is still important to follow through with the effort towards diagnosis. There are available means to test for problem genes that can be carriers of the genetic abnormality and many health institutions offer genetic testing regimens to identify these genes that can be causing heart illnesses in members of your family. Some of the common genetic illnesses to test for include Arrhythmogenic Right Ventricular Disease (ARVD), Marfan Syndrome, Long QT Syndrome, and Hypertropic Cardiomyopathy (HCM) and studies are underway to discover and detect other potential generic heart problems.
Should you suspect your family to have a genetic predisposition to heart illnesses, it is critical to immediately undergo genetic testing for these cases. It is also important to get counseling to assist in accepting the disease and planning lifestyle choices on how to overcome these genetic abnormalities. If you and your family are in a good frame of mind, it makes it easier to plan on how to respond to the illness before it worsens.
Do not take genetic heart problems lightly; rather, it is extremely important to be prepared to adopt a healthier lifestyle to minimize the potential effects of the disease as much as possible. There are ample methods available to control the progress of the disease and as long as you are willing to commit yourself to sticking to proven lifestyle choices, you can be confident that you can live many years without suffering from the symptoms of genetic heart problems.
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