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本病系家族遗传性粒细胞核形异常疾病,国外报告约为1/1000～1/10000,国内报告不多,我院近年发现4例,经对患者定期追踪观察及家系调查报告如下:例1 男,54岁,1959年2月至1960年7月因
The disease is a familial inherited granulocytic karyotype abnormality. The foreign reports are about 1/1000 ~ 1/10000. There are not many reports in our country. Four cases were found in our hospital in recent years. The follow-up observations and pedigree investigation reports are as follows: Example 1 Male, 54 years old, from February 1959 to July 1960 due to