Burnside Rachel D
Department of Cytogenetics, Laboratory Corporation of America Holdings, Center for Molecular Biology and Pathology, Research Triangle Park, N.C., USA.
Cytogenet Genome Res. 2015;146(2):89-99. doi: 10.1159/000438708. Epub 2015 Aug 8.
Chromosome 22q11.21 contains a cluster of low-copy repeats (LCRs), referred to as LCR22A-H, that mediate meiotic non-allelic homologous recombination, resulting in either deletion or duplication of various intervals in the region. The deletion of the DiGeorge/velocardiofacial syndrome interval LCR22A-D is the most common recurrent microdeletion in humans, with an estimated incidence of ∼1:4,000 births. Deletion of other intervals in 22q11.21 have also been described, but the literature is often confusing, as the terms 'proximal', 'nested', 'distal', and 'atypical' have all been used to describe various of the other intervals. Individuals with deletions tend to have features with widely variable expressivity, even among families. This review concisely delineates each interval and classifies the reported literature accordingly.
22号染色体q11.21区域包含一组低拷贝重复序列(LCRs),称为LCR22A - H,它们介导减数分裂非等位基因同源重组,导致该区域不同区间的缺失或重复。DiGeorge/心面综合征区间LCR22A - D的缺失是人类最常见的反复发生的微缺失,估计发病率约为1:4000活产儿。22q11.21其他区间的缺失也有报道,但文献往往令人困惑,因为“近端”“嵌套”“远端”和“非典型”等术语都曾用于描述其他不同的区间。即使在家族中,缺失个体的特征也往往具有广泛可变的表达性。本综述简要描述了每个区间,并据此对已发表的文献进行分类。