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伴有7号染色体单体的骨髓发育异常和白血病综合征:遗传学视角

Myelodysplasia and leukemia syndrome with monosomy 7: a genetic perspective.

作者信息

Gilchrist D M, Friedman J M, Rogers P C, Creighton S P

机构信息

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

出版信息

Am J Med Genet. 1990 Mar;35(3):437-41. doi: 10.1002/ajmg.1320350323.

Abstract

Acquired monosomy 7 is a frequent finding in myelodysplastic syndromes, including acute myelogenous leukemia. A subset of these patients has been described with an apparently distinct condition: myelodysplasia and leukemia syndrome with monosomy 7 (MLSM7). We report 2 brothers, 3 and 5 years of age, with MLSM7 and review other reports of familial occurrence. Genetic factors appear to be important in the cause of MLSM7, but the reported families do not fit neatly into any monogenic pattern. Recognition of the frequently familial nature of this condition requires hematological evaluation and genetic counseling for the families of patients with MLSM7.

摘要

获得性单体7是骨髓增生异常综合征(包括急性髓系白血病)中常见的发现。已描述了这些患者中的一部分患有明显不同的疾病:伴有单体7的骨髓发育异常和白血病综合征(MLSM7)。我们报告了2名分别为3岁和5岁的患有MLSM7的兄弟,并回顾了其他家族性发病的报告。遗传因素似乎在MLSM7的病因中很重要,但报告的家族并不完全符合任何单基因模式。认识到这种疾病常具有家族性,需要对MLSM7患者的家族进行血液学评估和遗传咨询。

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