| Literature DB >> 34801643 |
Camille Malouf1, Stephen J Loughran2, Adam C Wilkinson3, Akiko Shimamura4, Paula Río5.
Abstract
Bone marrow failure syndromes encompass a range of inherited and acquired hematological diseases that result in insufficient blood cell production, which leads to severe complications including anemia, weakening of the immune system, impaired coagulation, and increased risk of cancer. Within inherited bone marrow failure syndromes, a number of genetically distinct diseases have been described including Shwachman-Diamond syndrome and Fanconi anemia. Given the genetic complexity and poor prognosis of these inherited bone marrow failure syndromes, there is increasing interest in both characterizing the genetic landscapes of these diseases and developing novel gene therapies to effectively monitor and cure patients. These topics were the focus of the winter 2021 International Society for Experimental Hematology New Investigator Webinar, which featured presentations by Dr. Akiko Shimamura and Dr. Paula Río. Here, we review the topics covered within this webinar.Entities:
Mesh:
Year: 2021 PMID: 34801643 PMCID: PMC9165438 DOI: 10.1016/j.exphem.2021.11.004
Source DB: PubMed Journal: Exp Hematol ISSN: 0301-472X Impact factor: 3.249