Wolff-Parkinson-White Syndrome
"Wolff-Parkinson-White 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 form of ventricular pre-excitation characterized by a short PR interval and a long QRS interval with a delta wave. In this syndrome, atrial impulses are abnormally conducted to the HEART VENTRICLES via an ACCESSORY CONDUCTING PATHWAY that is located between the wall of the right or left atria and the ventricles, also known as a BUNDLE OF KENT. The inherited form can be caused by mutation of PRKAG2 gene encoding a gamma-2 regulatory subunit of AMP-activated protein kinase.
Descriptor ID |
D014927
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MeSH Number(s) |
C14.280.067.780.977 C14.280.123.750.977 C16.131.240.400.980
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Concept/Terms |
Wolff-Parkinson-White Syndrome- Wolff-Parkinson-White Syndrome
- Syndrome, Wolff-Parkinson-White
- Wolff Parkinson White Syndrome
- Auriculoventricular Accessory Pathway Syndrome
- WPW Syndrome
- Syndrome, WPW
- Ventricular Pre-Excitation with Arrhythmia
- Wolf-Parkinson-White Syndrome
- Syndrome, Wolf-Parkinson-White
- Wolf Parkinson White Syndrome
- Anomalous Ventricular Excitation Syndrome
- False Bundle-Branch Block Syndrome
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Below are MeSH descriptors whose meaning is more general than "Wolff-Parkinson-White Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Wolff-Parkinson-White Syndrome".
This graph shows the total number of publications written about "Wolff-Parkinson-White Syndrome" by people in this website by year, and whether "Wolff-Parkinson-White Syndrome" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1995 | 1 | 1 | 2 |
1996 | 1 | 0 | 1 |
2001 | 0 | 2 | 2 |
2002 | 0 | 1 | 1 |
2004 | 1 | 0 | 1 |
2005 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
2010 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2012 | 2 | 0 | 2 |
2014 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2017 | 2 | 0 | 2 |
2018 | 1 | 0 | 1 |
2019 | 1 | 0 | 1 |
2020 | 2 | 0 | 2 |
2021 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Wolff-Parkinson-White Syndrome" by people in Profiles.
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Rare Variant in MRC2 Associated With Familial Supraventricular Tachycardia and Wolff-Parkinson-White Syndrome. Circ Genom Precis Med. 2024 Aug; 17(4):e004614.
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Clinical Predictors of Recurrent Supraventricular Tachycardia in Infancy. J Am Coll Cardiol. 2022 09 20; 80(12):1159-1172.
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Routine Outpatient Electrocardiogram: What Is the Diagnosis? Tex Heart Inst J. 2021 01 01; 48(1).
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Loss of ventricular preexcitation during noninvasive testing does not exclude high-risk accessory pathways: A multicenter study of WPW in children. Heart Rhythm. 2020 10; 17(10):1729-1737.
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Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. Am J Med Genet A. 2020 06; 182(6):1387-1399.
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Association of Wolff-Parkinson-White With Left Ventricular Noncompaction Cardiomyopathy in Children. J Card Fail. 2019 Dec; 25(12):1004-1008.
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Efficacy of Nifekalant in Patients With Wolff-Parkinson-White Syndrome and Atrial Fibrillation: Electrophysiological and Clinical Findings. J Am Heart Assoc. 2019 07 02; 8(13):e012511.
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Utility and safety of adenosine challenge for subtle ventricular pre-excitation in the pediatric population. J Cardiovasc Electrophysiol. 2019 07; 30(7):1036-1041.
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Adenosine-sensitive Wolff-Parkinson-White: Longer time across the atrioventricular groove. Pacing Clin Electrophysiol. 2018 01; 41(1):35-41.
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Cardiac manifestations of PRKAG2 mutation. BMC Med Genet. 2018 01 03; 19(1):1.