Long QT Syndrome
"Long QT Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME.
Descriptor ID |
D008133
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MeSH Number(s) |
C14.280.067.565 C16.131.240.400.715 C23.550.073.547
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Long QT Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Long QT Syndrome".
This graph shows the total number of publications written about "Long QT Syndrome" by people in this website by year, and whether "Long QT Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 1 | 0 | 1 | 1997 | 1 | 0 | 1 | 1998 | 1 | 0 | 1 | 1999 | 1 | 0 | 1 | 2000 | 2 | 1 | 3 | 2002 | 0 | 1 | 1 | 2005 | 1 | 0 | 1 | 2006 | 2 | 0 | 2 | 2007 | 1 | 2 | 3 | 2008 | 5 | 1 | 6 | 2009 | 1 | 0 | 1 | 2012 | 2 | 0 | 2 | 2013 | 2 | 0 | 2 | 2014 | 1 | 0 | 1 | 2015 | 5 | 0 | 5 | 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Long QT Syndrome" by people in Profiles.
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Khan S, Berul CI. Long QT syndrome: Who needs a transplant? Heart Rhythm. 2017 08; 14(8):1189-1190.
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Berul CI. Shocking numbers--Reeducation to reduce inappropriate ICD utilization for congenital long QT syndrome. Heart Rhythm. 2016 Apr; 13(4):886-7.
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Czosek RJ, Kaltman JR, Cassedy AE, Shah MJ, Vetter VL, Tanel RE, Wernovksy G, Wray J, Marino BS. Quality of Life of Pediatric Patients With Long QT Syndrome. Am J Cardiol. 2016 Feb 15; 117(4):605-610.
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Greene EA, Punnoose A. Sports-Related Sudden Cardiac Injury or Death. Adolesc Med State Art Rev. 2015 Dec; 26(3):507-27.
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Kaltman JR, Berul CI. Attention-Deficit Hyperactivity Disorder and Long-QT Syndrome: Risky Business. J Cardiovasc Electrophysiol. 2015 Oct; 26(10):1045-7.
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Costello JP, Wilson JK, Louis C, Peer SM, Zurakowski D, Nadler EP, Qureshi FG, Jonas RA, Greene EA, Berul CI, Moak JP, Nath DS. Surgical cardiac denervation therapy for treatment of congenital ion channelopathies in pediatric patients: a contemporary, single institutional experience. World J Pediatr Congenit Heart Surg. 2015 Jan; 6(1):33-8.
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Seyerle AA, Young AM, Jeff JM, Melton PE, Jorgensen NW, Lin Y, Carty CL, Deelman E, Heckbert SR, Hindorff LA, Jackson RD, Martin LW, Okin PM, Perez MV, Psaty BM, Soliman EZ, Whitsel EA, North KE, Laston S, Kooperberg C, Avery CL. Evidence of heterogeneity by race/ethnicity in genetic determinants of QT interval. Epidemiology. 2014 Nov; 25(6):790-8.
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Miyake CY, Davis AM, Motonaga KS, Dubin AM, Berul CI, Cecchin F. Infant ventricular fibrillation after ST-segment changes and QRS widening: a new cause of sudden infant death? Circ Arrhythm Electrophysiol. 2013 Aug; 6(4):712-8.
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Burns KM, Greene EA. Long QT syndrome unmasked by dexmedetomidine: a case report. Congenit Heart Dis. 2014 Jan-Feb; 9(1):E11-5.
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He D, Costello JP, Nadler EP, Moak JP, Jonas RA, Nath DS. Left thoracoscopic sympathectomy used as primary therapy for a young child with intractable long QT syndrome. Pediatr Cardiol. 2013; 34(8):1969-71.
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