3号染色体短臂部分缺失:对3p25-3pter综合征的进一步描述

• 作 者: 郭立荣
• 出 处: 国外医学.遗传学分册
• 发表日期: 1987年04期
• 关键词: 短臂 ter 先天异常 新病例 超声检查 非近亲结婚 胎儿窘迫 二维心脏超声 细胞遗传学 发育不全

从1978年Verjaal等首次报道3号染色体短臂缺失以来,已经报道过几例3p综合征。然而,还没有确定该综合征的全部临床特征。作者报道1例具有多发性先天异常的新病例。以前认为这些异常与该综合征无关。

A few cases of 3p syndrome have been reported since the first report by Verjaal et al. In 1978 on the short arm of chromosome 3. However, the full clinical features of the syndrome have not yet been determined. The authors report a new case of multiple congenital anomalies. It was previously thought that these abnormalities had nothing to do with the syndrome.