小儿血液肿瘤学中的遗传综合征

V. M. Kozlova, Ekaterina E. Zelenova, T. T. Valiev, V. V. Semenova, T. V. Nasedkina, S. Mikhailova
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引用次数: 0

摘要

在儿童恶性肿瘤结构中,血液肿瘤疾病居首位。肿瘤克隆细胞中的体细胞突变已被充分研究,并被纳入现代分类中,用于将患者分为预后风险组和选择治疗方案。与此同时,50 多种与血母细胞瘤发病相关的遗传综合征已被描述。其中一些(唐氏综合征、克雷菲尔特综合征、微缺失综合征等)是由染色体病变引起的,而另一些则描述了一个或多个基因的改变,其遗传类型和血液肿瘤疾病的表现年龄各不相同。易患血液肿瘤疾病的基因涉及 DNA 修复过程、细胞周期调节、免疫反应和骨髓功能。本文介绍了与血细胞增多症发病有关的遗传综合征的最新数据,并描述了自己的临床观察结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hereditary syndromes in pediatric hematooncology
Hematooncological diseases head the list in the structure of malignant neoplasms of childhood. Somatic mutations in tumor clone cells have been well studied, included in modern classifications, and are used to stratify patients into prognostic risk groups and select a therapy program. At the same time, more than 50 hereditary syndromes associated with the development of hemoblastoses have been described. Some of them (Down’s syndrome, Klinefelter’s syndrome, microdeletion syndromes et al.) are caused by chromosomal pathology, while others describe alterations of one or more genes with different types of inheritance and age of manifestation of hematooncological diseases. Genes of predisposition to hematooncological diseases are involved in the processes of DNA repair, regulation of the cell cycle, immune response and bone marrow function. This article presents current data on genetic syndromes associated with the development of hemoblastosis with a description of their own clinical observations.
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