Brugada-Syndrom
Well, Olivia Christina (2011): Risikostratifizierung bei Patienten mit Brugada-Syndrom. Dissertation, LMU München: Medizinische Fakultät
... Eine Mutation im SCN5A‐Gen konnte nur bei einem von 9 Patienten mit Synkopen (11%) festgestellt
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Patienten,
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positive Familienanamnese für ein ...
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Electrical Storms in Brugada Syndrome: Review of Pharmacologic and Ablative Therapeutic Options
... the Brugada syndrome were monomorphic in all, coming from the RVOT in three patients (left bundle branch-inferior axis morphology, coupling interval of 343 ± 59 ms) and with left bundle branch block-superior axis ...
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Brugada Syndrome Associated With Adolescent Loperamide Abuse
... We present the case of a 14-year-old boy with obesity, hypertension, and chronic loperamide abuse who presented to our facility with symptoms of opioid withdrawal and type 1 Brugada pattern on an ...
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<p>Brugada syndrome: updated perspectives</p>
... Figure 3 Epicardial ablation of a Brugada syndrome patient. (A) Baseline type 2 ECG pattern visible with CARTO maps displaying abnormally prolonged potentials (210 ms) as purple, potentials between 110 and 200 ms ...
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Suspicion and Persistence: A Case of Pediatric Brugada Syndrome
... diagnosis. Brugada syndrome typically presents in adult men, is more often seen in those of Asian descent, and rarely manifests in ...the Brugada sign on baseline ...
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A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease
... Brugada syndrome (BrS) is a primary electrical heart disease, which can lead to sudden cardiac death. In older patients with BrS, the disease may coexist with ischaemic heart disease (IHD) and recent studies ...
5
Brugada syndrome in a family with a high mortality rate: a case report
... Brugada syndrome (BrS) is a hereditary arrhythmia char- acterized by a specific electrocardiographic (ECG) pat- tern and an increased risk of sudden cardiac death, with an apparent absence of structural ...
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Brugada Syndrome Masquerading as Febrile Seizures
... This case serves as a reminder that occult cardiac channelopathies should be borne in mind in the inves- tigation of childhood seizures with or without fever. However, we would not yet advise that all children who have a ...
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Effect of the Brugada syndrome mutation A39V on calmodulin regulation of Cav1.2 channels
... Results: We examined a Cav1.2 point mutant in the N-terminus region of the channel (A39V) that has been previously linked to Brugada syndrome. Using mutant CaM constructs in which the N- and/or C-lobe calcium ...
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Why It Is Important to Recognize Brugada Syndrome: A Case Report and Literature Review
... Introduction: Brugada syndrome is a rare, but serious clinical entity that is the leading cause of sudden cardiac death in young healthy ...with Brugada syndrome are caused by re- current ventricular ...
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Prognosis after Implantation of Cardioverter Defibrillators in Korean Patients with Brugada Syndrome
... Purpose: Our study aims to analyze prognosis after implantable cardioverter-defi- brillator (ICD) implantation in Korean patients with Brugada syndrome (BrS). Materials and Methods: This was a retrospective study ...
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Characterization of a novel Nav1.5 channel mutation, A551T, associated with Brugada syndrome
... (Nav1.5). Here, we characterized the biophysical properties of a novel Brugada syndrome- associated Nav1.5 mutation, A551T, identified in a proband who was successfully resuscitated from an episode of ventricular ...
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Schäfer, Stefan (2007): Genotyp-Phänotyp-Korrelation bei Long-QT-Syndrom und Brugada-Syndrom: Eine systematische Analyse an vier ausgewählten Fällen. Dissertation, LMU München: Medizinische Fakultät
... beim Brugada-Syndrom aufgrund des hohen Anteils negativer genetischer Befunde bei symptomatischen Patienten bislang nicht ...für Brugada-Syndrom-Patienten mit einer Mutation im Gen SCN5A kein ...
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Brugada Syndrome: A Review
... develop Brugada syndrome phenotype [13]. Brugada syndrome susceptibility genes were also found among calcium channels (CACNA1C, CACNB2b and ...of Brugada syndrome ...of Brugada syndrome ...
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Brugada syndrome
... Brugada syndrome (BrS; OMIM 601144), or "Idiopathic ventricular fibrillation" as defined by some authors [1], is an autosomal dominant form of cardiac arrhythmia, pre- senting with a typical ...
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Sudden Cardiac Arrest While Eating a Hot Dog: A Rare Presentation of Brugada Syndrome in a Child
... with Brugada syndrome (BS) usually experience sudden cardiac arrest (SCA) and arrhythmia when they have a high fever, consume alcohol, and, more frequently, during their night ...
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Role of pharmacotherapy in Brugada syndrome
... Brugada syndrome is a unique form of idiopathic ventricular fibrillation (VF), and is characterized by an ECG pattern with right bundle branch block (J wave), ST-segment elevation and terminal T-wave inversion in ...
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May Fever Trigger Ventricular Fibrillation?
... the Brugada syndrome in each case were noted at presentation and gradually returned to normal as fever ...the Brugada electrocardiographic pattern was not reproducible by pharmacologic testing in all ...
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Learning from studying very rare cardiac conditions: the example of short QT syndrome
... Genetic forms of SQTS are rare, but the condition may be under-diagnosed and carries a risk of sudden death. Genotyping of SQTS patients has led to identification of clear ion channel/transporter culprits in < 30% of ...
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Genetics of inherited primary arrhythmia disorders
... Abstract: A sudden unexplained death is felt to be due to a primary arrhythmic disorder when no structural heart disease is found on autopsy, and there is no preceding documentation of heart disease. In these cases, ...
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