Division of Medical Genetics, Department of Pediatrics, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Am J Med Genet A. 2013 Aug;161A(8):1992-8. doi: 10.1002/ajmg.a.35918.
An array-CGH on 19-year-old male showed a proximal 1.11 Mb duplication and a distal 1.7 Mb deletion of 22q11.2 regions flanking the Velocardiofacial/DiGeorge syndrome region that remained intact. FISH analyses revealed both abnormalities to be on the same homolog 22. This double rearrangement lead to the co-existence of two syndromes: Cat eye and distal 22q11.2 microdeletion syndromes with a rare associated phenotype of oculo-auriculo-vertebral spectrum (OAVS). A review of the literature indicates that this is the second report of a proximal duplication and the fifth report of a distal deletion and OAVS suggestive of a possible OAVS candidate gene in this region.
一份对 19 岁男性的 array-CGH 检测显示,22q11.2 区域的近端 1.11Mb 重复和远端 1.7Mb 缺失,该区域侧翼为室间隔缺损/ DiGeorge 综合征区域,保持完整。FISH 分析显示这两种异常均位于同一条 22 号染色体同源物上。这种双重重排导致了两种综合征的共存:猫眼和远端 22q11.2 微缺失综合征,以及一种罕见的眼-耳-脊椎综合征(OAVS)相关表型。文献回顾表明,这是第二次报道近端重复,第五次报道远端缺失和 OAVS,提示该区域可能存在 OAVS 候选基因。