Cervenka J, Hansen C A, Franciosi R A, Gorlin R J
J Med Genet. 1977 Aug;14(4):288-90. doi: 10.1136/jmg.14.4.288.
The case of a 10-month-old girl with an extra G-like chromosome is presented. Quinacrine, trypsin-Giemsa, and reverse banding identified the extra chromosome as no. 22. The phenotype of the patient is unique in that unilateral iris coloboma was observed, unlike the 18 cases of full trisomy 22 already published. This represents the first reported case of full trisomy 22 with this coloboma, or 'cat eye' anomaly, which is usually associated with partial trisomy 22. It is suggested that the use of the term 'cat eye syndrome' be revised. The terms 'partial trisomy 22 syndrome' and 'trisomy 22 syndrome' should be used instead.
本文报告了一例10个月大的女孩,其存在一条额外的类G染色体。喹吖因、胰蛋白酶-吉姆萨和反向显带技术鉴定出这条额外的染色体为22号染色体。该患者的表型独特,出现了单侧虹膜缺损,这与已发表的18例22号染色体完全三体患者不同。这是首例报道的伴有这种虹膜缺损或“猫眼”异常的22号染色体完全三体病例,这种异常通常与22号染色体部分三体相关。建议修订“猫眼综合征”这一术语,应改用“22号染色体部分三体综合征”和“22号染色体三体综合征”。