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An inferential study of the phenotype for the chromosome 15q24 microdeletion syndrome: a bootstrap analysis

机译:15q24染色体微缺失综合征表型的推断研究:自举分析

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摘要

In January 2012, a review of the cases of chromosome 15q24 microdeletion syndrome was published. However, this study did not include inferential statistics. The aims of the present study were to update the literature search and calculate confidence intervals for the prevalence of each phenotype using bootstrap methodology. Published case reports of patients with the syndrome that included detailed information about breakpoints and phenotype were sought and 36 were included. Deletions in megabase (Mb) pairs were determined to calculate the size of the interstitial deletion of the phenotypes studied in 2012. To determine confidence intervals for the prevalence of the phenotype and the interstitial loss, we used bootstrap methodology. Using the bootstrap percentiles method, we found wide variability in the prevalence of the different phenotypes (3–100%). The mean interstitial deletion size was 2.72 Mb (95% CI [2.35–3.10 Mb]). In comparison with our work, which expanded the literature search by 45 months, there were differences in the prevalence of 17% of the phenotypes, indicating that more studies are needed to analyze this rare disease.
机译:2012年1月,发表了有关15q24号染色体微缺失综合征病例的综述。但是,该研究未包括推论统计。本研究的目的是使用引导方法更新文献检索并计算每种表型患病率的置信区间。寻求该综合征患者的已发表病例报告,其中包括有关断点和表型的详细信息,其中包括36例。确定兆碱基(Mb)对中的缺失,以计算2012年研究的表型间质缺失的大小。为了确定表型患病率和间质损失的置信区间,我们使用了引导法。使用引导百分位数方法,我们发现不同表型的患病率差异很大(3–100%)。平均间隙缺失大小为2.72 Mb(95%CI [2.35-3.10 Mb])。与我们的研究(将文献检索时间延长了45个月)相比,表型的患病率存在​​差异,这表明需要更多的研究来分析这种罕见疾病。

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