Literature DB >> 22311567

Congenital long-QT syndrome in Addison's disease: a novel association.

Sean M Lang1, Nancy L Rollinson, Steven B Fishberger.   

Abstract

This report describes a teenager found to have both Addision's disease and long-QT syndrome type 1. This association is unique, but congenital long-QT channelopathies have been associated with other endocrinopathies. It remains to be seen whether genetic investigation should be performed for all patients with long-QTc's and endocrinopathies.

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Year:  2012        PMID： 22311567     DOI： 10.1007/s00246-012-0163-5

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN： 0172-0643            Impact factor:   1.655


  10 in total

1.  Co-morbidities, management and clinical outcome of auto-immune Addison's disease.

Authors:  Lalantha Leelarathna; Louise Breen; James K Powrie; Stephen M Thomas; Rustom Guzder; Barbara McGowan; Paul V Carroll
Journal:  Endocrine       Date:  2010-07-03       Impact factor: 3.633

2.  Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals.

Authors:  Ilan Goldenberg; Samuel Horr; Arthur J Moss; Coeli M Lopes; Alon Barsheshet; Scott McNitt; Wojciech Zareba; Mark L Andrews; Jennifer L Robinson; Emanuela H Locati; Michael J Ackerman; Jesaia Benhorin; Elizabeth S Kaufman; Carlo Napolitano; Pyotr G Platonov; Silvia G Priori; Ming Qi; Peter J Schwartz; Wataru Shimizu; Jeffrey A Towbin; G Michael Vincent; Arthur A M Wilde; Li Zhang
Journal:  J Am Coll Cardiol       Date:  2011-01-04       Impact factor: 24.094

3.  Lethal arrhythmia and corticosteroid insufficiency.

Authors:  Shinya Nishizawa; Takeshi Nakamura; Tetsuro Hamaoka; Akiyoshi Matsumuro; Takahisa Sawada; Hiroaki Matsubara
Journal:  Am J Emerg Med       Date:  2009-11       Impact factor: 2.469

Review 4.  Cardiac arrhythmia and thyroid dysfunction: a novel genetic link.

Authors:  Kerry Purtell; Torsten K Roepke; Geoffrey W Abbott
Journal:  Int J Biochem Cell Biol       Date:  2010-08-03       Impact factor: 5.085

5.  Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.

Authors:  Jamie D Kapplinger; David J Tester; Benjamin A Salisbury; Janet L Carr; Carole Harris-Kerr; Guido D Pollevick; Arthur A M Wilde; Michael J Ackerman
Journal:  Heart Rhythm       Date:  2009-06-23       Impact factor: 6.343

6.  Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.

Authors:  Suraj Kapa; David J Tester; Benjamin A Salisbury; Carole Harris-Kerr; Manish S Pungliya; Marielle Alders; Arthur A M Wilde; Michael J Ackerman
Journal:  Circulation       Date:  2009-10-19       Impact factor: 29.690

7.  Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.

Authors:  Grace Choi; Laura J Kopplin; David J Tester; Melissa L Will; Carla M Haglund; Michael J Ackerman
Journal:  Circulation       Date:  2004-10-04       Impact factor: 29.690

Review 8.  Long QT Syndrome.

Authors:  Ilan Goldenberg; Wojciech Zareba; Arthur J Moss
Journal:  Curr Probl Cardiol       Date:  2008-11       Impact factor: 5.200

9.  Torsade de pointes associated with recurrent ampulla cardiomyopathy in a patient with idiopathic ACTH deficiency.

Authors:  Naoki Gotyo; Michiya Kida; Toshiyuki Horiuchi; Yukio Hirata
Journal:  Endocr J       Date:  2009-06-09       Impact factor: 2.349

10.  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
  10 in total

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