Brugada syndrome is a genetic disorder in which an abnormality in the heart's electrical system causes life-threatening heart rhythm disturbances (arrhythmiasBrugada syndrome is characterized by ST-segment abnormalities in leads V1-V3 on ECG and a high risk of ventricular arrhythmias and sudden death.
Brugada syndrome presents primarily during adulthood. Brugada syndrome is a condition that causes a disruption of the heart's normal rhythm. This disorder can lead to uncoordinated electrical activity in the heart's lower chambers (ventricles), an abnormality called ventricular arrhythmia.
These complications typically occur when an affected person is resting or asleep. Brugada syndrome is an inherited condition that occurs most often in men. It also occurs with increased frequency in Asians. Brugada syndrome usually becomes apparent in adulthood, although signs and symptoms, including sudden death, can occur any time from early infancy to old age. Brugada syndrome most commonly affects otherwise healthy men aged 30-50 years. It is characterized by sudden and unexplained death, usually during sleep. Brugada syndrome may be inherited as an autosomal dominant trait.
Treatment here generally included implantation of an implantable defibrillator (ICD). This device oblige a pacemaker and is designed to restore the normal heart beat by delivering an electrical shock. This therapy does not cure the disease, but is meant to prevent sudden death. For high-risk individuals, treatment may include an implantable defibrillator. This small device continuously monitors your heart rhythm and delivers precisely calibrated electrical shocks when needed to control abnormal heartbeats. A Class Ia antiarrythmic drug, for decreasing VF episodes occurring in this syndrome.
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