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ECG pattern in Brugada syndrome. According to consensus guidelines, Type 1 ST segment elevation, either spontaneously present or induced with the sodium channel-blocker challenge test, is considered diagnostic. Type 2 and 3 may lead to suspicion, but provocation testing is required for diagnosis.
Long QT syndrome is estimated to affect 1 in 7,000 people. [6] Females are affected more often than males. [6] Most people with the condition develop symptoms before they are 40 years old. [6] It is a relatively common cause of sudden death along with Brugada syndrome and arrhythmogenic right ventricular dysplasia. [3]
A 2011 autopsy-based study found that sudden death was attributed to a cardiac condition in 79.3% of cases, and was unexplained in 20.7%. [3] In the Philippines, sudden adult death syndrome (or in their term, bangungot) is mainly caused by the Brugada syndrome. [14]
Short QT syndrome (SQT) is a very rare genetic disease of the electrical system of the heart, and is associated with an increased risk of abnormal heart rhythms and sudden cardiac death. [1] The syndrome gets its name from a characteristic feature seen on an electrocardiogram (ECG) – a shortening of the QT interval .
This is followed by sudden cardiac death in the absence of treatment. [2] Ventricular fibrillation is initially found in about 10% of people with cardiac arrest. [1] Ventricular fibrillation can occur due to coronary heart disease, valvular heart disease, cardiomyopathy, Brugada syndrome, long QT syndrome, electric shock, or intracranial ...
Antley–Bixler syndrome: Barth syndrome: Brugada syndrome: Cantú syndrome: genetic (Chromosome 12, autosomal dominant) Cardiac syndrome X: Cardiorenal syndrome: Kidney Cat eye syndrome: CHARGE syndrome: Coffin–Lowry syndrome: genetic (RPS6KA3 gene mutation, Chromosome X) Costello syndrome: Down syndrome: genetic (Chromosome 21) Dressler ...
Brugada syndrome is typically diagnosed using an electrocardiogram (ECG), although medications such as ajmaline may be required to produce the characteristic ECG pattern. [1] There is no cure for Brugada syndrome, but the condition may be treated using an implantable cardioverter defibrillator (ICD). [3]
Brugada syndrome. Preliminary "red flags" are identified that are more likely to suggest chest pain associated with heart. These are: past or current history of congentital or acquired heart disease; fainting when the child exerts herself or himself; an abnormality of blood coagulation that increases the risk of blood clots