Literature DB >> 15851440

Near-miss SIDS due to Brugada syndrome.

J R Skinner1, S-K Chung, D Montgomery, C H McCulley, J Crawford, J French, M I Rees.   

Abstract

A 19 day old infant was successfully resuscitated from ventricular fibrillation. The 12 lead ECG was normal, with a normal QT interval, and remains so over three years follow up. DNA analysis revealed a missense mutation (R1193Q) in the SCN5A gene, previously linked with familial sudden unexpected nocturnal death syndrome, also known as Brugada syndrome.

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Year:  2005        PMID: 15851440      PMCID: PMC1720395          DOI: 10.1136/adc.2004.058115

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  22 in total

1.  Is there a relation between SIDS and long QT syndrome?

Authors:  J R Skinner
Journal:  Arch Dis Child       Date:  2005-05       Impact factor: 3.791

Review 2.  Brugada syndrome in childhood: a potential fatal arrhythmia not always recognised by paediatricians. A case report and review of the literature.

Authors:  Yvan Mivelaz; Stefano Di Bernardo; Etienne Pruvot; Erik Jan Meijboom; Nicole Sekarski
Journal:  Eur J Pediatr       Date:  2006-05-03       Impact factor: 3.183

3.  Extracorporeal Life Support as a Rescue Measure for Managing Life-Threatening Arrythmia and Brugada Syndrome.

Authors:  Asaad G Beshish; Allison Weinberg; Waseem Ostwani; Gabe E Owens
Journal:  J Extra Corpor Technol       Date:  2017-12

4.  Nav1.5/R1193Q polymorphism is associated with both long QT and Brugada syndromes.

Authors:  H Huang; Juan Zhao; Fatima-Zahra Barrane; Jean Champagne; Mohamed Chahine
Journal:  Can J Cardiol       Date:  2006-03-15       Impact factor: 5.223

Review 5.  Brugada syndrome.

Authors:  Charles Antzelevitch
Journal:  Pacing Clin Electrophysiol       Date:  2006-10       Impact factor: 1.976

Review 6.  SIDS: genetic and environmental influences may cause arrhythmia in this silent killer.

Authors:  Jonathan C Makielski
Journal:  J Clin Invest       Date:  2006-02       Impact factor: 14.808

7.  Sudden infant death syndrome in mice with an inherited mutation in RyR2.

Authors:  Nitin Mathur; Subeena Sood; Sufen Wang; Ralph J van Oort; Satyam Sarma; Na Li; Darlene G Skapura; J Henri Bayle; Miguel Valderrábano; Xander H T Wehrens
Journal:  Circ Arrhythm Electrophysiol       Date:  2009-12

8.  Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome.

Authors:  David W Van Norstrand; David J Tester; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2008-02-16       Impact factor: 6.343

Review 9.  Neonatal tachycardias: an update.

Authors:  D S Kothari; J R Skinner
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2006-03       Impact factor: 5.747

Review 10.  Brugada syndrome: recent advances and controversies.

Authors:  Charles Antzelevitch; Eyal Nof
Journal:  Curr Cardiol Rep       Date:  2008-09       Impact factor: 2.931

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