Results 31 to 40 of about 10,650 (163)

Brugada Phenocopy Induced by Hypovolemic Hyponatremia. [PDF]

open access: yesCureus, 2023
Brugada syndrome (BrS) is a hereditary channelopathy caused by an autosomal dominant mutation in the cardiac sodium channel gene SCN5A alpha subunit. In individuals without structural heart disease, the risk of sudden cardiac death (SCD) increases in this channelopathy with ST-segment elevation in V1-3 precordials.
Yılmaz E, Özdemir F.
europepmc   +3 more sources

Brugada Phenocopy Caused by Intracranial Hemorrhage. [PDF]

open access: yesCureus, 2023
Brugada syndrome (BrS) is a congenital channelopathy associated with an increased risk of malignant ventricular arrhythmias and sudden cardiac death in individuals without any structural cardiopathy. Brugada phenocopies (BrPs) are clinical entities that present electrocardiographic patterns similar to those of BrS that are elicited only under ...
Branco T   +4 more
europepmc   +3 more sources

Brugada phenocopy in a child with pediatric inflammatory multisystemic syndrome caused by SARS-CoV-2. [PDF]

open access: yesRev Esp Cardiol (Engl Ed), 2022
Brugada syndrome (BS) is an inherited channelopathy associated with elevated risk of ventricular fibrillation and sudden cardiac death. Its diagnosis is based on a standard electrocardiographic pattern comprising ST-segment elevation 2 mm in right ...
Santiago-Cortés R   +5 more
europepmc   +2 more sources

Not All Brugada Electrocardiogram Patterns are Brugada Syndrome or Brugada Phenocopy

open access: yesBalkan Medical Journal, 2017
We thank Dr. Arı and Ekici for using the term Brugada phenocopies in their literature; however, we would like to emphasise that Brugada electrocardiogram patterns induced by sodium channel blockers should not be classified as Brugada phenocopies.
Grace Xu   +3 more
doaj   +4 more sources

Brugada Phenocopy That Lurks After Hemodialysis: A Case Report

open access: yesIndian Journal of Clinical Cardiology, 2022
Brugada phenocopies (BrP) are clinical commodities that are etiologically distinguishable from genuine congenital Brugada syndrome. BrP is marked by type-1 or type-2 Brugada electrocardiogram (ECG) patterns in precordial V1 to V3, which is provoked by ...
Hendsun Hendsun   +2 more
doaj   +1 more source

Hypophosphatemia causing ST elevation in a critically ill noncardiac surgery postoperative patient

open access: yesAnnals of Noninvasive Electrocardiology, Volume 27, Issue 4, July 2022., 2022
Abstract The patient is a 73‐year‐old female with peripheral vascular disease, coronary artery disease, and systemic lupus erythematosus, who underwent mesenteric artery bypass surgery. She suffered from a pneumonia after surgery, causing acute hypoxic respiratory failure and septic shock. Due to shock, she developed acute renal failure.
Joey Junarta, Gregary D. Marhefka
wiley   +1 more source

Sudden Cardiac Arrest in the Paediatric Population

open access: yesCJC Pediatric &Congenital Heart Disease, Volume 1, Issue 2, Page 45-59, April 2022., 2022
Abstract Sudden cardiac arrest in the young is a rare event with a range of potential causes including cardiomyopathies, ion channelopathies, and autonomic nervous system dysfunction. Investigations into the cause involve a multidisciplinary team, including cardiologists, geneticists, and psychologists. In addition to a detailed medical history, family
Sonia Franciosi   +3 more
wiley   +1 more source

Transgenic rabbit models for cardiac disease research

open access: yesBritish Journal of Pharmacology, Volume 179, Issue 5, Page 938-957, March 2022., 2022
To study the pathophysiology of human cardiac diseases and to develop novel treatment strategies, complex interactions of cardiac cells on cellular, tissue and on level of the whole heart need to be considered. As in vitro cell‐based models do not depict the complexity of the human heart, animal models are used to obtain insights that can be translated
Tibor Hornyik   +7 more
wiley   +1 more source

A Case of Brugada Phenocopy in Adrenal Insufficiency-Related Pericarditis

open access: yes, 2022
This is a report of a 27-year-old man with known history of Addison’s disease, noncompliant with medications, and hypothyroidism who presented with shortness of breath, nausea, vomiting, fever, and chest pain as well as Brugada sign seen on ...
Asllanaj, Blerina   +10 more
core   +1 more source

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