Factor X deficiency in the neonatal period. [PDF]
Archives of Disease in Childhood, 1980 An infant with a severe deficiency of factor X presened in the neonatal period with uncontrollable bleeding from heel prick sites, spontaneous bruising, and haematoma. The deficiency was controlled by infusions of dried human factors II, IX, and X concentrate; the half-life of the infused factor X material is only 18 hours.
M R Winter +3 more
openaire +4 more sources
Staged Surgical Palliation for HLHS in a Girl with Severe Factor X Deficiency
The Thoracic & Cardiovascular Surgeon Reports, 2018 Background Factor X deficiency (also known as Stuart–Prower factor deficiency) is an autosomal recessive extremely rare hereditary hematologic disorder, affecting around 1:1,000,000 of the general population.
Ahmed F. Elmahrouk +6 more
doaj +2 more sources
Rate-limiting roles of the tenase complex of factors VIII and IX in platelet procoagulant activity and formation of platelet-fibrin thrombi under flow [PDF]
Haematologica, 2015 The importance of factor Xa generation in thrombus formation has not been studied extensively so far. Here, we used mice deficient in either factor VIII or factor IX to determine the role of platelet-stimulated tenase activity in the formation of ...
Frauke Swieringa +4 more
doaj +5 more sources
A viable mouse model of factor X deficiency provides evidence for maternal transfer of factor X. [PDF]
, 2008 BackgroundActivated factor X (FXa) is a vitamin K-dependent serine protease that plays a pivotal role in blood coagulation by converting prothrombin to thrombin. There are no reports of humans with complete deficiency of FX, and knockout of murine F10 is
Arruda, VR +7 more
core +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 +2 more sources
PERAWATAN GIGI DAN MULUT PENDERITA HEMOFILIA [PDF]
Journal of Dentistry Indonesia, 2015 Haemophilia is a congenital haemorrhagic disorders passed down by the x linked recessive, divided into two: Haemophilia A caused by deficiency of factor VIII and Haemophilia B caused by deficiency of factor IX.
Siti Marhamah
doaj +3 more sources
FACTOR-X DEFICIENCY: A RARE DISORDER TO BE LOOKED FOR IN CASES OF CONGENITAL BLEEDING TENDENCY [PDF]
Khyber Medical University Journal, 2018 Factor X deficiency is a rare, autosomal recessive disorder that involves the coagulation cascade. People with this disorder present with a myriad of early life bleeding complications.
Fatima Ayaz +2 more
doaj +3 more sources
PB2326: SAFE AND EFFECTIVE PROPHYLAXIS WITH PLASMA-DERIVED FACTOR X CONCENTRATE IN AN ELDERLY PATIENT WITH HEREDITARY FACTOR X DEFICIENCY [PDF]
HemaSphere, 2022 H. Patel +3 more
doaj +2 more sources
Pediatric split liver transplantation for congenital factor X deficiency: first 10-year follow-up of a case with portal vein stenting [PDF]
Korean J Transplant, 2021 Jung‐Man Namgoong +7 more
openalex +3 more sources
Cardiac Amyloidosis Presenting with Pre-Excitation Syndrome, Heart Failure, and Severe Factor X Deficiency as Part of Systemic Amyloid Light-Chain (AL) Amyloidosis – A Fatal Combination [PDF]
Am J Case Rep, 2021 Hussam Almasri +11 more
openalex +3 more sources