"Romano-Ward 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 long QT syndrome that is without congenital deafness. It is caused by mutation of the KCNQ1 gene which encodes a protein in the VOLTAGE-GATED POTASSIUM CHANNEL.
| Descriptor ID |
D029597
|
| MeSH Number(s) |
C14.280.067.565.720 C14.280.123.625.720 C16.131.240.400.715.720 C23.550.073.547.720
|
| Concept/Terms |
Romano-Ward Syndrome- Romano-Ward Syndrome
- Romano Ward Syndrome
- Syndrome, Romano-Ward
- Ventricular Fibrillation with Prolonged QT Interval
- Long QT Syndrome Type 1
- Long QT Syndrome 1
- Ward-Romano Syndrome
- Syndrome, Ward-Romano
- Ward Romano Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Romano-Ward Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Romano-Ward Syndrome".
This graph shows the total number of publications written about "Romano-Ward Syndrome" by people in this website by year, and whether "Romano-Ward Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
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Below are the most recent publications written about "Romano-Ward Syndrome" by people in Profiles.
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Hoefen R, Reumann M, Goldenberg I, Moss AJ, O-Uchi J, Gu Y, McNitt S, Zareba W, Jons C, Kanters JK, Platonov PG, Shimizu W, Wilde AA, Rice JJ, Lopes CM. In silico cardiac risk assessment in patients with long QT syndrome: type 1: clinical predictability of cardiac models. J Am Coll Cardiol. 2012 Nov 20; 60(21):2182-91.
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Barsheshet A, Goldenberg I, O-Uchi J, Moss AJ, Jons C, Shimizu W, Wilde AA, McNitt S, Peterson DR, Zareba W, Robinson JL, Ackerman MJ, Cypress M, Gray DA, Hofman N, Kanters JK, Kaufman ES, Platonov PG, Qi M, Towbin JA, Vincent GM, Lopes CM. Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to ?-blocker therapy in type 1 long-QT syndrome. Circulation. 2012 Apr 24; 125(16):1988-96.
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Casimiro MC, Knollmann BC, Yamoah EN, Nie L, Vary JC, Sirenko SG, Greene AE, Grinberg A, Huang SP, Ebert SN, Pfeifer K. Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans. Genomics. 2004 Sep; 84(3):555-64.