Brugada Syndrome: Recognize the Silent Risk Causes, symptoms, ECG diagnosis, treatment
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How ICD Saves a Life in Brugada Syndrome | Ventricular Fibrillation Explained
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Brugada syndrome is an inherited arrhythmia disorder caused by SCN5A gene mutations that impair sodium channel function. The condition may first present as syncope, seizure-like activity, or even sudden death, often without any structural heart disease. The type 1 Brugada pattern on ECG is only diagnostic in the presence of symptoms. Without them, it’s the Brugada sign, which still warrants follow-up but not necessarily intervention. Want more cardiology visuals? Follow us and explore: https://m
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Brugada Synonym - Brugada syndrome (BrS) is a rare, inherited genetic disorder that disrupts the heart's normal rhythm and can cause life-threatening irregular heartbeats. #cardio #cardiologists #cardiovascular #cardiologist #cardiology #cardiovasculardisease #mbbsstudent #mbbsdiaries #mbbs #mbbsstudents #mbbsnotes #mbbslife #medical #medicalstudents #medicalknowledge #medicalscience #medicalmarijuana #medicos #medico #nursinglife #nursingstudent #nursingschool #nursing #viralreels #viralpost #v
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I was diagnosed with autoimmune hypothyroidism at age 21. I’m 48 now, so this has been part of my body for 27 years. What most people don’t realize is the thyroid and the stomach are closely linked in autoimmunity. When one is affected, the other often follows. There’s even a clinical name for it (thyrogastric syndrome) first described in the 1960s. A recent bidirectional endoscopy revealed autoimmune gastritis. It’s the same underlying autoimmune tendency I’ve lived with since 21, now showing u
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