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Overview of inherited bone marrow failure syndromes

Patients with inherited bone marrow failure syndrome (IBMFS) can develop peripheral blood cytopenia, which can ultimately progress to myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML). Although some cases of IBMFS are diagnosed based on their typical presentation, variable disease penet...

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Autor principal: Park, Meerim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057667/
https://www.ncbi.nlm.nih.gov/pubmed/35483926
http://dx.doi.org/10.5045/br.2022.2022012
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author Park, Meerim
author_facet Park, Meerim
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description Patients with inherited bone marrow failure syndrome (IBMFS) can develop peripheral blood cytopenia, which can ultimately progress to myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML). Although some cases of IBMFS are diagnosed based on their typical presentation, variable disease penetrance and expressivity may result in diagnostic dilemmas. With recent advances in genomic evaluation including next-generation sequencing, many suspected cases of IBMFS with atypical presentations can be identified. Identification of the genetic causes of IBMFS has led to important advances in understanding DNA repair, telomere biology, ribosome biogenesis, and hematopoietic stem cell regulation. An overview of this syndromes is summarized in this paper.
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spelling pubmed-90576672022-05-10 Overview of inherited bone marrow failure syndromes Park, Meerim Blood Res Review Article Patients with inherited bone marrow failure syndrome (IBMFS) can develop peripheral blood cytopenia, which can ultimately progress to myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML). Although some cases of IBMFS are diagnosed based on their typical presentation, variable disease penetrance and expressivity may result in diagnostic dilemmas. With recent advances in genomic evaluation including next-generation sequencing, many suspected cases of IBMFS with atypical presentations can be identified. Identification of the genetic causes of IBMFS has led to important advances in understanding DNA repair, telomere biology, ribosome biogenesis, and hematopoietic stem cell regulation. An overview of this syndromes is summarized in this paper. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2022-04-30 2022-04-30 /pmc/articles/PMC9057667/ /pubmed/35483926 http://dx.doi.org/10.5045/br.2022.2022012 Text en © 2022 Korean Society of Hematology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Park, Meerim
Overview of inherited bone marrow failure syndromes
title Overview of inherited bone marrow failure syndromes
title_full Overview of inherited bone marrow failure syndromes
title_fullStr Overview of inherited bone marrow failure syndromes
title_full_unstemmed Overview of inherited bone marrow failure syndromes
title_short Overview of inherited bone marrow failure syndromes
title_sort overview of inherited bone marrow failure syndromes
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057667/
https://www.ncbi.nlm.nih.gov/pubmed/35483926
http://dx.doi.org/10.5045/br.2022.2022012
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