Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency [PDF]
Due to a homozygous Gly204Arg mutation in the factor X (FX) gene no detectable FX antigen was found in the plasma of a one-year old patient with severe bleeding diathesis.
Zsuzsanna Bereczky+7 more
doaj +5 more sources
Neonatal presentation of factor X deficiency
Factor X is a Vitamin K-dependent serine protease synthesized in the liver. It is a key factor of the coagulation cascade as it is the first enzyme of a common pathway that leads to the formation of a stable fibrin clot.
Arjani Patra+3 more
doaj +3 more sources
A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female [PDF]
Factor X deficiency is a rare coagulopathy that can be inherited or acquired. Acquired factor X deficiency has been associated with plasma cell dyscrasias, amyloids, and use of vitamin K antagonists.
Ayrton Bangolo+6 more
doaj +2 more sources
1. Dorothy M (Adcock) Funk, M.D.[⇑][1] 1. Esoterix Coagulation, 8490 Upland Drive, Ste.100, Englewood, CO 80112 2. Dennis Casciato, M.D. 1. David Geffen School of Medicine at UCLA, Los Angeles, CA 90095-1732 1. Address for Correspondence: Dorothy M (Adcock) Funk, M.D., Esoterix Coagulation, 8490 Upland Drive, Ste.100, Englewood, CO ...
Dennis A. Casciato+1 more
openaire +3 more sources
Factor X Deficiency and Pregnancy [PDF]
©Factor X deficiency is a rare disorder, with only 50 cases reported to date. There are only a few published case reports of women with Factor X deficiency undergoing successful pregnancy, each with a unique clinical course and approach to management. In this case report, we review the literature on Factor X deficiency and pregnancy.
Donna Castellone+4 more
openaire +3 more sources
A viable mouse model of factor X deficiency provides evidence for maternal transfer of factor X [PDF]
Background:Activated factor X (FXa) is a vitamin K-dependent serine protease that plays a pivotal role in blood coagulation by converting prothrombin to thrombin.
ARRUDA, V R+7 more
core +4 more sources
Acquired-Transient Factor X Deficiency in a Teenager with Extensive Burns [PDF]
Acquired factor X deficiency is an extremely rare situation. It has shown to be associated with systemic amyloidosis, respiratory mycoplasma infection, factor X inhibitors, antiphospholipid antibodies, vitamin K defi ciency/liver disease as well as the ...
Almeida, T+3 more
core +3 more sources
Fatal acquired coagulation factor V deficiency after hepatectomy for advanced hepatocellular carcinoma as a possible immune checkpoint inhibitor-related adverse event: a case report [PDF]
Background Atezolizumab plus bevacizumab therapy was recently introduced as the first line for unresectable advanced hepatocellular carcinoma (HCC), but immune-related adverse events (IrAEs) due to atezolizumab are a great concern.
Shintaro Arakaki+13 more
doaj +2 more sources
Diagnosis and treatment of inherited factor X deficiency [PDF]
Summary. Factor X is a vitamin K‐dependent, liver‐produced serine protease that serves a pivotal role in coagulation as the first enzyme in the common pathway to fibrin formation. Inherited factor X deficiency is a rare autosomal recessive bleeding disorder that is estimated to occur in 1:1 000 000 individuals up to 1:500 carriers.
Peter A. Kouides, Deborah L. Brown
openaire +3 more sources
Combined Factor VII and X Deficiency [PDF]
Factor VII deficiency and factor X deficiency and very rare disorders individually. Combined Factor VII and X is a rare congenital blood disorder with very few cases reported in the literature.
Gursharan Singh Narang,+2 more
doaj +1 more source