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

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

Open Access
|Jul 2022

Abstract

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.

DOI: https://doi.org/10.34763/jmotherandchild.20222601.d-22-00002 | Journal eISSN: 2719-535X | Journal ISSN: 2719-6488
Language: English
Page range: 104 - 110
Submitted on: Jan 12, 2022
Accepted on: Apr 5, 2022
Published on: Jul 20, 2022
Published by: Institute of Mother and Child
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2022 Emir Behluli, Nexhibe Nuhii, Thomas Liehr, Gazmend Temaj, published by Institute of Mother and Child
This work is licensed under the Creative Commons Attribution 4.0 License.