Institute for Medical and Human Genetics, Charité Universitätsmedizin Berlin, Berlin, Germany.
Am J Med Genet A. 2013 Jan;161A(1):218-24. doi: 10.1002/ajmg.a.35695. Epub 2012 Dec 14.
Distal 15q25.2 microdeletions have recently been reported as a copy number variation (CNV) locus for neurodevelopmental and neuropsychiatric disorders with variable outcome. In addition, more proximal microdeletions of 15q25.2 have been described as a susceptibility locus for cognitive deficits, congenital diaphragmatic hernia (CDH), and Diamond-Blackfan anaemia (DBA). We describe two patients with 15q25.2 deletion, one with the more distal deletion and the other with a deletion overlapping both the distal and proximal 15q25.2 deletions and compare them to the 18 so far reported patients with 15q25.2 deletions. We provide a characterization of the 15q25.2 microdeletions and contribute to the genotype-phenotype delineation for these two novel microdeletion syndromes.
远端 15q25.2 微缺失最近被报道为神经发育和神经精神疾病的拷贝数变异(CNV)位点,其结果存在差异。此外,更近端的 15q25.2 微缺失已被描述为认知缺陷、先天性膈疝(CDH)和 Diamond-Blackfan 贫血(DBA)的易感位点。我们描述了两名 15q25.2 缺失患者,一名患者有更远端的缺失,另一名患者有远端和近端 15q25.2 缺失重叠的缺失,并将其与迄今为止报道的 18 名 15q25.2 缺失患者进行比较。我们对 15q25.2 微缺失进行了特征描述,并为这两种新型微缺失综合征进行了基因型-表型描绘。