A Sardinian Family with Factor XI Deficiency.

CONCLUSION: A mixing test of a prolonged aPTT should be performed because it will be present both in patients with or without the inhibitor. A molecular analysis in severe FXI deficiency is warranted as it may have prognostic significance. CWA may be helpful for better understanding the pathophysiology of this kind of defect. PMID: 31364091 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31364091?dopt=Abstract

Source: Hamostaseologie - July 29, 2019 Category: Hematology Authors: Barcellona D, Favuzzi G, Vannini ML, Piras SM, Ruberto MF, Grandone E, Marongiu F Tags: Hamostaseologie Source Type: research