Romano-Ward Syndrome
"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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Below are the most recent publications written about "Romano-Ward Syndrome" by people in Profiles.
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Cuneo BF, Strasburger JF. We only find what we look for: fetal heart rate and the diagnosis of long-QT syndrome. Circ Arrhythm Electrophysiol. 2015 Aug; 8(4):760-2.