唐氏综合征患者急性淋巴细胞白血病基因遗传的怀疑。

Emir Behluli, Nexhibe Nuhii, Thomas Liehr, Gazmend Temaj
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引用次数: 1

摘要

患有唐氏综合症(DS)的儿童患急性淋巴细胞白血病(ALL)的风险明显增加。在美国,每732名新生儿中就有1人患有21号染色体三体症。ALL是儿童中最常见的癌症,约占15岁以下儿童癌症诊断的25%。儿科急性淋巴细胞白血病的治疗和管理方案不同;然而,与没有DS的儿童相比,患有ALL的DS-ALL儿童的治疗相关毒性风险增加。在此,我们总结了所有遗传易感性的现有文献,以及DS-ALL患者的分子治疗和治疗的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome.

Children with Down syndrome (DS) are at markedly increased risk for acute lymphoblastic leukaemia (ALL). DS is caused by trisomy of chromosome 21 affecting approximately 1 in 732 newborns in the USA. ALL is the most common cancer in children and constitutes approximately 25% of cancer diagnoses among children under the age of 15. Different protocols for treatment and management of paediatric ALL are available; however, DS children with ALL (DS-ALL) have increased risk of therapy-related toxicity compared to those without DS. Herein, we summarize the available literature on inherited predisposition for ALL, and possibilities for molecular therapy and treatment for DS-ALL patients.

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