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Overview of inherited bone marrow failure syndromes
Blood Research ; : S49-S54, 2022.
Article em En | WPRIM | ID: wpr-925629
Biblioteca responsável: WPRO
ABSTRACT
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.
Texto completo: 1 Índice: WPRIM Tipo de estudo: Prognostic_studies Idioma: En Revista: Blood Research Ano de publicação: 2022 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Tipo de estudo: Prognostic_studies Idioma: En Revista: Blood Research Ano de publicação: 2022 Tipo de documento: Article