Results 11 to 20 of about 2,202,317 (252)

Brugada Syndrome.

JACC: Clinical Electrophysiology, 2022
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and cardiac arrest, predominantly during sleep. The prevalence is ∼1:2,000, and is more commonly diagnosed in young to middle-aged males, although patient sex does not appear to impact prognosis.
A. D. Krahn, Elijah R Behr, R. Hamilton, Vincent Probst, Zachary Laksman, Hui-Chen Han   +5 more
semanticscholar   +3 more sources

Experimental Models of Brugada syndrome [PDF]

International Journal of Molecular Sciences, 2019
Brugada syndrome is an inherited, rare cardiac arrhythmogenic disease, associated with sudden cardiac death. It accounts for up to 20% of sudden deaths in patients without structural cardiac abnormalities.
F. Sendfeld, E. Selga, F. Scornik, G. J. Pérez, Nicholas L Mills, Ramon Brugada   +5 more
semanticscholar   +6 more sources

Fever as a Catalyst for Life-Threatening Arrhythmias in Brugada Syndrome: A Rare Case of Brugada Syndrome Unmasked in a Young Male. [PDF]

Clin Case Rep
ABSTRACT Brugada syndrome (BrS) is a rare, genetically predisposed arrhythmic disorder associated with an elevated risk of sudden cardiac death (SCD) due to ventricular arrhythmias. Fever is a recognized trigger that can unmask the Type 1 Brugada electrocardiogram (ECG) pattern and precipitate life‐threatening arrhythmias, even in individuals without ...
Khalil I, Hossain MI.
europepmc   +2 more sources

Brugada syndrome [PDF]

Orphanet Journal of Rare Diseases, 2006
A novel clinical entity characterized by ST segment elevation in right precordial leads (V1 to V3), incomplete or complete right bundle branch block, and susceptibility to ventricular tachyarrhythmia and sudden cardiac death has been described by Brugada et al. in 1992. This disease is now frequently called "Brugada syndrome" (BrS).
Napolitano C, PRIORI, SILVIA GIULIANA
openaire   +7 more sources

Brugada Syndrome

Gomal Journal of Medical Sciences, 2013
The Brugada syndrome is a genetic disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death.1 it is named by the Spanish cardiologists Pedro Brugada and Joseph Brugada.
Syed Azhar Sherazi, Muhammad Rehan Khan
doaj   +2 more sources

Clinical Features of Brugada Syndrome Patients With SCN5A Variants. [PDF]

J Cardiovasc Electrophysiol
Longer r‐J interval in lead V1, fragmented QRS and carrying SCN5A variants other than benign variants are independently associated with the cardiac events in BrS patients. LAS40 and RMS40 are useful for the risk stratification in BrS patients with SCN5A VUS or pathogenic variants.
Okamura S, Ochi H, Nakashima M, Akiyama R, Tokuyama T, Okubo Y, Miyauchi S, Miyamoto S, Oguri N, Uotani Y, Sakai T, Furutani M, Kihara Y, Nakano Y.   +13 more
europepmc   +2 more sources

Brugada Syndrome

The Lancet, 2002
Charles Antzelevitch, Pedro Brugada, Josép Brugada, Ramón Brugada, Wataru Shimizu, Ihor Gussak, Andrés Ricardo Pérez‐Riera   +6 more
openalex   +3 more sources

Sumatriptan Induced Brugada Syndrome, a Rare Presentation of a Commonly Used Drug [PDF]

Clin Case Rep
ABSTRACT We aim to highlight an important and rare association of Brugada Syndrome with a commonly used medication, Sumatriptan, which is used as an aborting Migraine headaches. This life‐threatening condition needs early diagnosis and prompt management with vigilant follow‐up for better patient outcomes.
Iqbal P, Monfared S, Sacoto D, Ozbay M, Abdelmottaleb W, Caballero V, Tahir M, Mushiyev S.   +7 more
europepmc   +2 more sources

Long-term of epicardial radiofrequency ablation and benefit for recurrent ventricular arrhythmia in Brugada syndrome: A systematic review and meta-analysis. [PDF]

J Arrhythm
Epicardial radiofrequency ablation significantly reduces recurrent ventricular arrhythmias and ICD shocks in Brugada syndrome, with excellent long‐term safety and no reported mortality. Epicardial ablation is an effective strategy for sustained rhythm stabilization. Abstract Background Brugada syndrome (BrS) is a rare cardiac channelopathy linked to an
Adji AS, Billah A, Sit JEP, de Liyis BG, Nugraha A, Puspita A, Satrioaji AM, Rosyadi RN.   +7 more
europepmc   +2 more sources

Brugada Syndrome [PDF]

Cardiogenetics, 2011
The Brugada syndrome demonstrates characteristic electrocardiogram features and is a significant cause of sudden death in young adults with overtly normal cardiac structure and function. The genetic basis has not yet been fully elucidated but our understanding of the causative mutations and modifiers of arrhythmic events is advancing rapidly alongside ...
Bastiaenen, Rachel, Behr, Elijah R.
openaire   +2 more sources