Structured Summary
Abstract
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.
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Classification
Broader headings
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MeSH Record
Synonyms
8 entry terms
- Long QT Syndrome 1
- Long QT Syndrome Type 1
- Ventricular Fibrillation with Prolonged QT Interval
- Ward-Romano Syndrome
- Romano Ward Syndrome
- Syndrome, Romano-Ward
- Syndrome, Ward-Romano
- Ward Romano Syndrome
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2002; use LONG QT SYNDROME 1986-2001
MeSH Record
Previous Indexing
- Long QT Syndrome (1985-2001)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Romano-Ward Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D029597. http://id.nlm.nih.gov/mesh/2026/D029597
- Romano-Ward Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Romano%E2%80%93Ward_syndrome
- Romano-Ward Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q724714