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Although many of those with Brugada syndrome do not have any symptoms, Brugada syndrome may cause fainting or sudden cardiac death due to serious abnormal heart rhythms, such as ventricular fibrillation or polymorphic ventricular tachycardia. [9] Blackouts may be caused by brief abnormal heart rhythms that revert to a normal rhythm spontaneously.
Rare diseases called ion channelopathies may play a role such as long QT syndrome (LQTS), Brugada syndrome (BrS), CPVT (catecholaminergic polymorphic ventricular tachycardia), progressive cardiac conduction defect (PCCD), early repolarization syndrome, mixed sodium channel disease, and short QT syndrome. [13]
Brown–Vialetto–Van Laere syndrome; Bruck syndrome; Brugada syndrome; Brunner syndrome; Budd–Chiari syndrome; Burning feet syndrome; Burning mouth syndrome; Burnside–Butler syndrome; Buschke–Ollendorff syndrome; Bálint's syndrome; Börjeson-Forssman-Lehmann syndrome
Bartter syndrome: various, by type Brugada syndrome: various, by type Catecholaminergic polymorphic ventricular tachycardia (CPVT) Ryanodine receptor: Congenital hyperinsulinism: Inward-rectifier potassium ion channel: Cystic fibrosis: Chloride channel Dravet syndrome: Voltage-gated sodium channel: Episodic ataxia: Voltage-gated potassium ...
Torsades de pointes, torsade de pointes or torsades des pointes (TdP; also called torsades) (/ t ɔːr ˌ s ɑː d d ə ˈ p w æ̃ t /, [2] French: [tɔʁsad də pwɛ̃t̪], translated as "twisting of peaks") is a specific type of abnormal heart rhythm that can lead to sudden cardiac death.
respiratory distress syndrome; measles; meconium aspiration syndrome; metapneumovirus (hMPV) infection; necrotizing enterocolitis; neonatal conjunctivitis; parainfluenza (PIV) infection; pertussis; poliomyelitis; prenatal Listeria; Group B streptoccus infection; Tay–Sachs disease; tetanus; Ureaplasma urealyticum infection; respiratory ...
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]
Romano–Ward syndrome increases the risk of abnormal heart rhythms or arrhythmias. These are typically a form of ventricular tachycardia known as Torsades de pointes which can cause faints, seizures, or even sudden death. [1] Less dangerous arrhythmias such as atrial fibrillation also occur, causing symptoms of heart racing or palpitations ...