| Literature DB >> 28093361 |
Rosa Romano1, Apostolos Zaravinos2, Kyriaki Liadaki1, Rozina Caridha1, Johanna Lundin3, Göran Carlsson4, Jacek Winiarski5, Qiang Pan-Hammarström1, Lennart Hammarström6.
Abstract
We report the first patient with an interstitial deletion of chromosome 15q24.1-q24.3 associated with common variable immunodeficiency (CVID). The 18-year old female patient's clinical and immunological phenotype was compared with 8 additional previously published patients with chr15q24 deletions. A CGH analysis estimated the deletion to be 3.767Mb in size (chr15: 74,410,916-78,178,418) and the result was confirmed using qRT-PCR. We defined an immune-related commonly deleted region (ICDR) within the chromosomal band 15q24.2, deleted in all four patients with different forms of antibody deficiencies. Mutations in the 14 genes within this ICDR were not identified in the remaining allele in our patient by WES and gene expression analyses showed haploinsufficiency of all the genes. Among these genes, we consider Nei Like DNA Glycosylase 1 (NEIL1) as a likely candidate gene due to its crucial role in B-cell activation and terminal differentiation.Entities:
Keywords: CVID; DNA repair; Exome sequencing; Immunodeficiency; chr15q24 deletion
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Year: 2017 PMID: 28093361 DOI: 10.1016/j.clim.2017.01.006
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969