FAQ

Romano-Ward Syndrome

Known as: Long QT Syndrome Type 1, LQT1, Romano Ward Syndrome 
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… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1976-2018
010203019762018

Related topics

Related topics

17 relations
Autosomal dominant inheritanceCardiovascular systemChestGenetic Heterogeneity
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Related mentions per year

Related mentions per year

1936-2019
19401960198020002020
Romano-Ward Syndrome
Chest
Respiratory System
radiotherapeutic
Autosomal dominant inheritance
Ventricular Fibrillation

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Comparison of the static and dynamic balance performance in young, middle-aged, and elderly healthy people.
BACKGROUND Body sway increases with age. The purpose of this study was to obtain baseline data and the characteristics of balance… (More)
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2008
2008
Improved Selection Operator for Ga
Selection operator is one of the important aspects in the GA process. There are several ways for selection. Some of them are… (More)
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2004
2004
Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans.
Inherited long QT syndrome is most frequently associated with mutations in KCNQ1, which encodes the primary subunit of a… (More)
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Highly Cited
2004
Highly Cited
2004
Exogenous and endogenous ghrelin in gastroprotection against stress-induced gastric damage.
Ghrelin, identified in the gastric mucosa has been involved in control of food intake and growth hormone (GH) release but little… (More)
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2004
2004
Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome.
Romano-Ward syndrome (RWS), the autosomal dominant form of the congenital long QT syndrome, is characterised by prolongation of… (More)
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Highly Cited
2004
Highly Cited
2004
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.
Wolcott-Rallison syndrome (WRS) is a rare autosomal-recessive disorder characterized by the association of permanent neonatal or… (More)
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Highly Cited
2003
Highly Cited
2003
LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)
AbstractHutchinson-Gilford progeria syndrome (HGPS; MIM 176670) is an extremely rare disease that is characterized by accelerated… (More)
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Highly Cited
2000
Highly Cited
2000
Differential effects of beta-adrenergic agonists and antagonists in LQT1, LQT2 and LQT3 models of the long QT syndrome.
OBJECTIVES To define the cellular mechanisms responsible for the development of life-threatening arrhythmias in response to… (More)
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Highly Cited
1997
Highly Cited
1997
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.
BACKGROUND KVLQT1, the gene encoding the alpha-subunit of a cardiac potassium channel, is the most common cause of the dominant… (More)
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1980
1980
[Romano Ward syndrome].
About syncopal attacks caused by cardial arrhythmias had been frequently reported. In one family we found female members of three… (More)
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