儿童哮喘的遗传方面:潜在的临床作用

IF 0.2 Q4 ALLERGY
Sarwat E Deraz
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引用次数: 0

摘要

支气管哮喘是一种引起呼吸困难的气道持续炎症性疾病。它是全世界慢性发病率和死亡率的一个主要原因,有证据表明,在过去20年中,其患病率显著增加,特别是在儿童中。儿童哮喘症状的患病率在不同人群中从1%到30%以上不等,并且在大多数国家都在增加。在埃及,哮喘是急诊和住院的最常见原因,3-15岁儿童的患病率估计为8.2%,死亡率每年增加10%。哮喘的遗传学在儿童哮喘中很重要。了解儿童哮喘的流行病学、发病机制、自然病史和管理需要现有的哮喘遗传方面的临床知识。确定与哮喘相关的基因为更好地确定其发病机制提供了一种手段,有望改善预防策略、诊断工具和治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic aspects of pediatric asthma: potential clinical role
Introduction Bronchial asthma is a disease of continuing inflammatory disorder of the airways that causes trouble breathing. It is a major cause of chronic morbidity and mortality throughout the world and there is evidence that its prevalence has increased considerably over the past 20 years especially in children .The prevalence of asthma symptoms in children varies from 1 to more than 30% in different populations and is increasing in most countries . In Egypt, asthma is the commonest cause of emergency and hospital admission where the prevalence among children aged 3-15 years estimated to be 8.2%, with 10% annual increase in mortality . The genetics of asthma is important in pediatric asthma. Current clinical Knowledge of genetic aspects of asthma is needed to understand the epidemiology, pathogenesis, natural history and management of children with asthma . Identifying the genes associated with asthma offers a means of better define of its pathogenesis, with the promise of improving preventive strategies, diagnostic tools and therapies .
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