Informaţii despre

Nume Brugada Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Other specified cardiac arrhythmias
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Brugada Syndrome 1; Brugada Syndrome 2; Brugada Syndrome 3; Brugada Syndrome 4; Brugada Syndrome 5; Brugada Syndrome 6; Brugada Syndrome 7; Brugada Syndrome 8; Brugada Syndrome 9

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Boli A-Z Acute Myocardial Infarction Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity Syndrome, Mild Aneurysm Aniridia 1 Anorexia Nervosa 1 Arrhythmogenic Right Ventricular Cardiomyopathy Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Atrial Fibrillation Atrial Standstill Atrial Standstill 1 Atrioventricular Block Autonomic Dysfunction Autonomic Neuropathy Blood Group--Ahonen Blood Group, Dombrock System Brugada Syndrome 1 Brugada Syndrome 2 Brugada Syndrome 5 Cantu Syndrome Cardiac Arrest Cardiac Arrhythmia Cardiac Conduction Defect Cardiac Conduction Disease with or Without Dilated Cardiomyopathy Cardiomyopathy, Dilated, 1o Catecholaminergic Polymorphic Ventricular Tachycardia Cellulitis Central Nervous System Origin Vertigo Cerebral Aneurysms Cerebritis Cholangiocarcinoma Coronary Artery Vasospasm Dyspepsia Early Repolarization Associated with Ventricular Fibrillation Elastosis Perforans Serpiginosa Epilepsy Erythromelalgia Fainting Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form Familial Long Qt Syndrome Familial Progressive Cardiac Conduction Defect Familial Short Qt Syndrome Familial Sick Sinus Syndrome Febrile Seizures Galactose Epimerase Deficiency Heart Conduction Disease Hepatic Adenomas, Familial Hyperkalemic Periodic Paralysis Hypertrophic Cardiomyopathy Hypokalemia Hypokalemic Periodic Paralysis, Type 1 Influenza Intrinsic Cardiomyopathy Ischemia Isolated Optic Neuritis Jervell and Lange-Nielsen Syndrome 1 Left Ventricular Noncompaction Leukemia Long Qt Syndrome Long Qt Syndrome 1 Long Qt Syndrome 12 Long Qt Syndrome 13 Long Qt Syndrome 2 Long Qt Syndrome 3 Long Qt Syndrome 5 Long Qt Syndrome 6 Long Qt Syndrome 9 Lowe Oculocerebrorenal Syndrome Malignant Spiradenoma Meckel Syndrome, Type 1 Monoclonal Mast Cell Activation Syndrome Mucolipidosis Ii Alpha/beta Mutism Myeloid Leukemia Myocardial Infarction Myotonic Dystrophy Naxos Disease Neuronitis Neuropathy Paroxysmal Extreme Pain Disorder Pemphigus Pemphigus Vulgaris Pericarditis Periodic Paralyses Pneumonia Postural Orthostatic Tachycardia Syndrome Prinzmetal's Variant Angina Progressive Familial Heart Block Progressive Familial Heart Block, Type Ia Progressive Familial Heart Block, Type Ib Pulmonary Embolism Right Bundle Branch Block Shigellosis Short Qt Syndrome Sick Sinus Syndrome Sleep Disorder Spinocerebellar Ataxia Type 19/22 Status Epilepticus Sudden Infant Death Syndrome Syncope Third-Degree Atrioventricular Block Timothy Syndrome Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy Wolff-Parkinson-White Syndrome