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A framework for understanding quality of life domains in individuals with the CDKL5 deficiency disorder

机译:用CDKL5缺乏症理解个体生活领域的质量的框架

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The CDKL5 deficiency disorder (CDD) is a rare condition caused by spontaneous mutations on the cyclin-dependent kinase-like 5 (CDKL5) gene. It is a severe and complex disability that markedly affects the individual's health and wellbeing. This study aimed to identify the quality of life (QOL) domains important for individuals with CDD. Twenty-five parents of individuals registered in the International CDKL5 Disorder Database participated in semi-structured telephone interviews to explore areas that supported or challenged their child's QOL. Rett syndrome (RTT) is another severe genetically-caused neurodevelopmental disorder but is generally less severe than CDD. Qualitative data were analysed using directed content analysis, based on previously identified QOL domains for RTT that related to health and wellbeing, daily activities and community immersion and services. Each of the domains identified for RTT was represented in the CDD dataset overall and when the dataset was divided into three age groups: 3-5 years old; 6-18years old; and older than 18years. This is the first study to conceptualise factors important for individuals with CDD. Findings from this study will guide health professionals and other service providers who support individuals with CDD and will offer insight into choosing appropriate QOL instruments when measuring outcomes for this group.
机译:CDK15缺陷障碍(CDD)是由细胞周期蛋白依赖性激酶样5(CDK15)基因的自发突变引起的罕见条件。这是一种严重而复杂的残疾,显着影响个人的健康和幸福。本研究旨在识别对CDD个体重要的生活质量(QOL)域名。在国际CDKL5紊乱数据库中注册的二十五名个人父母参加了半结构化电话采访,探索支持或挑战孩子QoL的地区。 Rett综合征(RTT)是另一种严重的遗传导致神经发育障碍,但通常比CDD严重。基于先前识别的RTT的QoL结构域,通过针对健康和福利,日常活动和社区浸入和服务的RTT的QoL结构域分析定性数据。 RTT确定的每个域在CDD数据集中表示,当数据集分为三个年龄组时:3-5岁; 6-18年的旧;比18年龄较大。这是第一次研究对CDD个人的概念性因素。本研究的调查结果将指导卫生专业人员和其他支持CDD个人的服务提供商,并在衡量该组的结果时选择适当的QOL仪器。

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