James C, Robson L, Jackson J, Smith A
Pediatrician Unit, Children's Hospital, Sydney, Australia.
Am J Med Genet. 1995 May 8;56(4):389-92. doi: 10.1002/ajmg.1320560408.
Chromosome analysis was performed on a 3-year-old boy because of bilateral radioulnar synostosis and demonstrated a mosaic karyotype 46,XY/47,XYY/48,XYYY. He had minor facial anomalies and mild intellectual delay. He appears to be the youngest patient reported with this rare chromosome complement. His father, mother, and brother had normal chromosomes. Fluorescence in situ hybridization (FISH) was performed on the propositus and his father with the Y chromosome heterochromatic probe (pHY3.4) to add to the evaluation of mosaicism.
由于双侧桡尺骨融合,对一名3岁男孩进行了染色体分析,结果显示为嵌合核型46,XY/47,XYY/48,XYYY。他有轻微的面部异常和轻度智力发育迟缓。他似乎是报道的具有这种罕见染色体组成的最年轻患者。他的父亲、母亲和哥哥染色体正常。对先证者及其父亲使用Y染色体异染色质探针(pHY3.4)进行了荧光原位杂交(FISH),以进一步评估嵌合现象。