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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 amon...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sciendo
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032328/ https://www.ncbi.nlm.nih.gov/pubmed/35853737 http://dx.doi.org/10.34763/jmotherandchild.20222601.d-22-00002 |
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author | Behluli, Emir Nuhii, Nexhibe Liehr, Thomas Temaj, Gazmend |
author_facet | Behluli, Emir Nuhii, Nexhibe Liehr, Thomas Temaj, Gazmend |
author_sort | Behluli, Emir |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10032328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Sciendo |
record_format | MEDLINE/PubMed |
spelling | pubmed-100323282023-03-23 Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome Behluli, Emir Nuhii, Nexhibe Liehr, Thomas Temaj, Gazmend J Mother Child Review Articles 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. Sciendo 2022-07-20 /pmc/articles/PMC10032328/ /pubmed/35853737 http://dx.doi.org/10.34763/jmotherandchild.20222601.d-22-00002 Text en © 2022 Emir Behluli et al., published by Sciendo https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. |
spellingShingle | Review Articles Behluli, Emir Nuhii, Nexhibe Liehr, Thomas Temaj, Gazmend Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome |
title | Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome |
title_full | Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome |
title_fullStr | Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome |
title_full_unstemmed | Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome |
title_short | Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome |
title_sort | suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndrome |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032328/ https://www.ncbi.nlm.nih.gov/pubmed/35853737 http://dx.doi.org/10.34763/jmotherandchild.20222601.d-22-00002 |
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