首页> 中文期刊>国际儿科学杂志 >遗传性骨髓衰竭综合征的研究进展

遗传性骨髓衰竭综合征的研究进展

摘要

遗传性骨髓衰竭综合征是一组先天性疾病.其发病机制尚不完全明确,目前已发现部分致病基因,而且初步掌握了其诊断和治疗方法.此类疾病的诊断多依据典型的临床表现及相关实验室检查.随着基因检测的开展,致病基因检测正成为确诊该类疾病的主要方法.目前造血干细胞移植是唯一可能治愈本疾病的方法,支持和对症治疗在延缓和改善病情方面至关重要,基因治疗尚不成熟,其他治疗手段均在不断探索中.%Inherited bone marrow failure syndromes are a group of congenital diseases.Their pathogenesis are not entirely clear.The causative genes have been found in part of the diseases, and we have preliminarily mastered their diagnosis and treatment.The diagnosis is mostly based on typical clinical manifestations and related laboratory tests.Along with the genetic testing developmenff,genetic testing has become the main method to diagnose IBMFS.Hematopoietic stem cell transplantation is currently the only way to cure these diseases.Support and symptomatic treatment also play an important role in terms of delaying and improving the condition.Gene therapy is still not mature, and other treatments are constantly being explored.

著录项

相似文献

  • 中文文献
  • 外文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号