Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation
Journal
International journal of hematology
Journal Volume
116
Journal Issue
4
Pages
528
Date Issued
2022-10
Author(s)
Lin, Ching-Yeh
Lin, Hsuan-Yu
Pai, Chen-Hsueh
Yu, Cheng-Ye
Kuo, Su-Feng
Lin, Jen-Shiou
Lin, Po-Te
Hung, Mei-Hua
Hsieh, Han-Ni
Liu, Hsiang-Chun
Abstract
Factor XII (FXII) deficiency is an interesting condition that causes prolonged activated partial thromboplastin time without bleeding diathesis. FXII may be not important in hemostasis, but still plays roles in thrombosis and inflammation. In order to raise clinical awareness about this condition, we studied patients with severe FXII deficiency and their relatives.
Subjects
Cross-reacting material; Factor XII deficiency; Factor XII gene; Factor XII gene mutation; Factor XII gene promoter polymorphism; Factor XII protein
Publisher
SPRINGER JAPAN KK
Type
journal article