American journal of medical genetics · 2000
Genetic aspects of arrhythmias.
СтатьяПоддержка исследования: вне правительства СШАПоддержка службы здравоохранения СШАОбзорНазвание и аннотация: Перевод в очереди
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Roberts R, Brugada R
Аннотация
Advances in the treatment and prevention of heart disease have led to consistently declining morbidity and mortality rates over the past 30 years. Despite these advances, therapy remains largely palliative. The development of curative therapies is limited by our lack of knowledge of the basic mechanisms of disease. In the next decade, we will probably change many of these current approaches from treating the crisis to preventing the disease. Molecular biology and genetics have elucidated several basic pathways. It is hoped that targeted therapies will prevent or arrest many of these cardiac diseases, in particular, arrhythmias and sudden death. With the discovery of the genes causing familial diseases like long QT, hypertrophic cardiomyopathy, and Brugada syndrome, we have identified several substrates responsible for triggering malignant arrhythmias.
Предметные рубрики MeSH
AdolescentAdultAnimalsArrhythmias, CardiacArrhythmogenic Right Ventricular DysplasiaAsia, SoutheasternAtrial FibrillationBundle-Branch BlockCardiomyopathy, HypertrophicChildChild, PreschoolChromosome MappingChromosomes, HumanDeath, Sudden, CardiacFemaleGenetic HeterogeneityGenetic LinkageGenetic TestingGenetic TherapyHeart Defects, CongenitalHumansHypertrophy, Left VentricularIncidenceInfantInfant, NewbornIon ChannelsIon TransportLong QT SyndromeMaleMiceModels, AnimalMutationNAV1.5 Voltage-Gated Sodium ChannelPhenotypePrevalenceRabbitsRiskSodium ChannelsSyndrome