"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 |
|---|
| 2018 | 3 | 0 | 3 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Romano-Ward Syndrome" by people in Profiles.
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Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene. Stem Cell Res. 2019 04; 36:101416.
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Electro-mechanical (dys-)function in long QT syndrome type 1. Int J Cardiol. 2019 Jan 01; 274:144-151.
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Functionally Aberrant Mutant KCNQ1 With Intermediate Heterozygous and Homozygous Phenotypes. Can J Cardiol. 2018 09; 34(9):1174-1184.
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Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1. Stem Cell Res. 2018 05; 29:170-173.