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Socioeconomic disparities in European cystic fibrosis outcomes: time to close the gap
European Respiratory Journal ( IF 24.3 ) Pub Date : 2024-03-07 , DOI: 10.1183/13993003.00328-2024
Edward F. McKone

Extract

Cystic fibrosis (CF) is one of the most common autosomal recessive genetic conditions that causes progressive lung disease and premature death [1]. Median survival worldwide is estimated to be around 50 years, but there is variation between countries [2–4]. Reasons for this variation are complex, and include genetic factors such as cystic fibrosis transmembrane conductance regulator (CFTR) genetic mutations in the population [5], as well as non-genetic factors such as access to lung transplantation and socioeconomic status (SES) [4].



中文翻译:

欧洲囊性纤维化结果的社会经济差异:是时候缩小差距了

提炼

囊性纤维化(CF)是最常见的常染色体隐性遗传病之一,可导致进行性肺病和过早死亡[1]。全球中位生存期估计约为 50 年,但各国之间存在差异 [2-4]。这种变异的原因很复杂,包括遗传因素,例如人群中囊性纤维化跨膜电导调节因子(CFTR)基因突变[5],以及非遗传因素,例如获得肺移植和社会经济地位(SES)[ 4]。

更新日期:2024-03-07
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