Schroeder Verena
Department for BioMedical Research (DBMR), University of Bern, Bern, Switzerland.
Hamostaseologie. 2020 Nov;40(4):467-471. doi: 10.1055/a-1181-0327. Epub 2020 Aug 31.
Laboratory diagnosis of congenital and acquired deficiencies of coagulation factor XIII (FXIII) can be challenging. Determination of FXIII function requires specific and sensitive assays which are not always available. This brief review article summarizes currently used FXIII assay methods, their principles and difficulties, and discusses the recommended diagnostic workup in case of a suspected FXIII deficiency. The article also briefly touches on experimental methods used in FXIII research.
先天性和获得性凝血因子 XIII(FXIII)缺乏症的实验室诊断可能具有挑战性。FXIII 功能的测定需要特定且灵敏的检测方法,而这些方法并非总是可得。这篇简短的综述文章总结了目前使用的 FXIII 检测方法、其原理和难点,并讨论了疑似 FXIII 缺乏症时推荐的诊断检查流程。文章还简要介绍了 FXIII 研究中使用的实验方法。