Literature DB >> 15929461

The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death in children and young adults.

G Michael Vincent1.   

Abstract

Inherited Long QT and Brugada syndromes cause syncope and sudden cardiac death due to ventricular tachyarrhythmias. Diagnosis may be difficult and the syncopal events are commonly misdiagnosed as neurally mediated (vaso-vagal) episodes or as "seizures". The details of the events (onset, offset, sequelae, precipitating factors) and knowledge of the ECG features are key to the correct diagnosis, and in assisting the neurologist in discriminating these two life-threatening disorders from neurally mediated (vaso-vagal) syncope and in discerning when a "seizure" might be due to a lethal cardiac arrhythmia. Very effective treatments are available and prompt, correct diagnosis and appropriate treatment are life-saving.

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Year:  2005        PMID: 15929461     DOI: 10.1016/j.spen.2004.11.008

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  9 in total

1.  Risk of recurrent cardiac events after onset of menopause in women with congenital long-QT syndrome types 1 and 2.

Authors:  Jonathan Buber; Jehu Mathew; Arthur J Moss; W Jackson Hall; Alon Barsheshet; Scott McNitt; Jennifer L Robinson; Wojciech Zareba; Michael J Ackerman; Elizabeth S Kaufman; David Luria; Michael Eldar; Jeffrey A Towbin; Michael Vincent; Ilan Goldenberg
Journal:  Circulation       Date:  2011-05-31       Impact factor: 29.690

2.  Predictors of heart-focused anxiety in patients undergoing genetic investigation and counseling of long QT syndrome or hypertrophic cardiomyopathy: a one year follow-up.

Authors:  Anniken Hamang; Geir Egil Eide; Berit Rokne; Karin Nordin; Cathrine Bjorvatn; Nina Øyen
Journal:  J Genet Couns       Date:  2011-07-20       Impact factor: 2.537

3.  Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome.

Authors:  Ilan Goldenberg; Arthur J Moss; Derick R Peterson; Scott McNitt; Wojciech Zareba; Mark L Andrews; Jennifer L Robinson; Emanuela H Locati; Michael J Ackerman; Jesaia Benhorin; Elizabeth S Kaufman; Carlo Napolitano; Silvia G Priori; Ming Qi; Peter J Schwartz; Jeffrey A Towbin; G Michael Vincent; Li Zhang
Journal:  Circulation       Date:  2008-04-21       Impact factor: 29.690

4.  Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice.

Authors:  Stephan E Lehnart; Marco Mongillo; Andrew Bellinger; Nicolas Lindegger; Bi-Xing Chen; William Hsueh; Steven Reiken; Anetta Wronska; Liam J Drew; Chris W Ward; W J Lederer; Robert S Kass; Gregory Morley; Andrew R Marks
Journal:  J Clin Invest       Date:  2008-06       Impact factor: 14.808

5.  Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndrome.

Authors:  Tao Yang; Seo-Kyung Chung; Wei Zhang; Jonathan G L Mullins; Caroline H McCulley; Jackie Crawford; Judith MacCormick; Carey-Anne Eddy; Andrew N Shelling; John K French; Ping Yang; Jonathan R Skinner; Dan M Roden; Mark I Rees
Journal:  Circ Arrhythm Electrophysiol       Date:  2009-05-22

6.  Sudden cardiac death in children and adolescents (excluding Sudden Infant Death Syndrome).

Authors:  Kelly K Gajewski; J Philip Saul
Journal:  Ann Pediatr Cardiol       Date:  2010-07

7.  General anxiety, depression, and physical health in relation to symptoms of heart-focused anxiety- a cross sectional study among patients living with the risk of serious arrhythmias and sudden cardiac death.

Authors:  Anniken Hamang; Geir E Eide; Berit Rokne; Karin Nordin; Nina Øyen
Journal:  Health Qual Life Outcomes       Date:  2011-11-14       Impact factor: 3.186

8.  Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2.

Authors:  Ewa Moric-Janiszewska; Joanna Głogowska-Ligus; Monika Paul-Samojedny; Ludmiła Węglarz; Grażyna Markiewicz-Łoskot; Lesław Szydłowski
Journal:  Arch Med Sci       Date:  2011-12-30       Impact factor: 3.318

9.  Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.

Authors:  Su Zhang; Ke Yin; Xiang Ren; Pengyun Wang; Shirong Zhang; Lingling Cheng; Junguo Yang; Jing Yu Liu; Mugen Liu; Qing Kenneth Wang
Journal:  BMC Med Genet       Date:  2008-04-09       Impact factor: 2.103

  9 in total

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