 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 |
|---|
| 2013 | 1 | 0 | 1 | | 2019 | 1 | 1 | 2 |
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Below are the most recent publications written about "Long QT Syndrome" by people in Profiles.
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Puri K, Malek J, de la Uz CM, Lantos J, Cabrera AG, Frugé E. Allowing Adolescents to Weigh Benefits and Burdens of High-stakes Therapies. Pediatrics. 2019 07; 144(1).
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Lantos JD. The False-negative Phenotype. Pediatrics. 2019 01; 143(Suppl 1):S33-S36.
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Tisma-Dupanovic S, Wagner JB, Shah S, Huang DT, Moss AJ. An adolescent with possible arrhythmogenic right ventricular dysplasia and long QT syndrome: evaluation and management. Ann Noninvasive Electrocardiol. 2013 Jan; 18(1):75-8.
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