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

4Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

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.

Cite

CITATION STYLE

APA

Palazón-Bru, A., Ramírez-Prado, D., Cortés, E., Aguilar-Segura, M. S., & Gil-Guillén, V. F. (2016). An inferential study of the phenotype for the chromosome 15q24 microdeletion syndrome: A bootstrap analysis. PeerJ, 2016(2). https://doi.org/10.7717/peerj.1641

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free