A Rare Cause of Acquired Factor X Deficiency in an 87-Year-Old Female [PDF]
Case Reports in Hematology, 2021 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 +5 more sources
Inherited Moderate Factor X Deficiency Presenting as Cardiac Tamponade [PDF]
Case Reports in Hematology, 2019 Factor X deficiency is a rare bleeding disorder that varies in the severity of its clinical manifestations. The symptoms of this disorder can occur at any age, although most severe cases appear in childhood.
Tamer Othman +4 more
doaj +5 more sources
Plasma‐derived factor X concentrate compassionate use for hereditary factor X deficiency: Long‐term safety and efficacy in a retrospective data‐collection study [PDF]
Research and Practice in Thrombosis and Haemostasis, 2021 Background Coagadex is a high‐purity plasma‐derived factor X concentrate (pdFX) developed to treat hereditary factor X deficiency (FXD). Objective Evaluate the efficacy and safety of pdFX administered to patients with hereditary FXD.
James N. Huang +4 more
doaj +3 more sources
Occurrence and management of severe bleeding episodes in patients with hereditary factor X deficiency. [PDF]
Haemophilia, 2021 Vitamin K–dependent factor X (FX) plays an important role in thrombin formation, and a deficiency in FX can cause impaired coagulation, the severity of which is usually correlated with the degree of deficiency.
Tarantino MD.
europepmc +4 more sources
Acquired Factor X Deficiency in Patients With Primary Light Chain Amyloidosis [PDF]
Journal of Investigative Medicine High Impact Case Reports, 2019 Acquired factor X (FX) deficiency is a rare but serious complication of primary amyloidosis, presumably caused by the binding of amyloid proteins to the clotting factors.
Siroj Dejhansathit MD +1 more
doaj +3 more sources
Diagnosis and treatment of inherited factor X deficiency [PDF]
Haemophilia, 2008 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.
Deborah Brown, Peter A. Kouides
semanticscholar +4 more sources
The Long-term Outcomes after VAD plus SCT Therapy in a Patient with AL Amyloidosis and Severe Factor X Deficiency. [PDF]
Intern Med, 2018 A 55-year-old man was admitted to our institute to undergo evaluation for proteinuria (5.4 g/day) with lambda-type Bence-Jones protein (BJP). Primary amyloid light chain (AL) amyloidosis and acquired factor X deficiency were diagnosed.
Iwadate D +16 more
europepmc +3 more sources
Successful treatment of a noninhibitory antibody-mediated acquired factor X deficiency in a patient with marginal-zone lymphoma. [PDF]
Clin Case Rep, 2015 Prolonged clotting times were observed in a patient with spontaneous hemorrhage. Analysis showed severe factor X deficiency due to clearance by a noninhibitory antibody.
Meenhuis A +5 more
europepmc +4 more sources
PB2319: ACQUIRED COAGULOPATHY: FACTOR X DEFICIENCY AT DIAGNOSIS OF MULTIPLE MYELOMA WITHOUT ASSOCIATED AMYLOIDOSIS [PDF]
HemaSphere, 2022 M. De La Torre De La Paz +6 more
doaj +3 more sources
A case report of congenital factor X deficiency in an adult patient [PDF]
SAGE Open Medical Case Reports, 2022 Factor X deficiency is one of the rarest coagulation disorders representing 10% of all rare bleeding diseases with a frequency of 1:1,000,000. A 39-year-old male patient with no previous medical conditions was admitted to the hospital with a left carpal ...
Rehab Y AL-Ansari +3 more
doaj +2 more sources