Below you will find more information about Arrhythmogenic Right Ventricular Cardiomyopathy from Medigest. If you believe that you are suffering from any of the symptoms of Arrhythmogenic Right Ventricular Cardiomyopathy it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Arrhythmogenic Right Ventricular Cardiomyopathy and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Arrhythmogenic Right Ventricular Cardiomyopathy comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is an genetic cardiac muscle disorder characterized by a damaged muscle that can be gradually replaced by fat and scar tissue. This serious heart disease is one of the highly recognized causes of sudden death among teenagers. ARVC can cause some abnormal heart rhythms that can result to the weakening of the heart's pumping action. In most cases, this medical condition is not fatal and does not significantly affect the quality of life. However, a number of patients usually develop some other complications and would require constant medical attention.
In order to make a definitive diagnosis of ARVD, there are a number of clinical tests to be performed including echocardiograpy, cardiac MRI, electro cardiogram and right ventricular angiography.
The common treatments for ARVC include the prescription of beta-blockers such as amiodarone or sotalol to effectively lower proarrhythmic risk. Some patients may also require implantable cardioverter defibrillator. Heart transplantation may also be considered in severe cases with patients in the end stage heart failure.
Symptoms and Signs
Among the prominent signs and symptoms of the progression of this disease includes subtle ventricular changes and arrhythmias. The involvement of both ventricular may possibly lead to heart failure and cardiomyopathy.
The underlying cause of ARVC is human genetics, typically inherited as a dominant Mendelian disease.Discuss Arrhythmogenic Right Ventricular Cardiomyopathy in our forums
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