What can cause clotting factor dysfunction or deficiency?

2-acetylaminofluorene dengue fever cirrhosis warfarin yellow fever cholestasis malabsorption liver failure Viral hemorrhagic fever Haemophilia A asparaginase Kasabach-Merritt syndrome Haemorrhagic disease of the newborn Phenprocoumon Acenocoumarol Phenindione heparin Reye's syndrome von Willebrand disease tissue plasminogen activator Rivaroxaban antithrombin fondaparinux streptokinase Vitamin K deficiency Haemophilia B argatroban Lassa fever urokinase Bivalirudin Haemophilia C Lepirudin dicoumarol Haem arginate Tenecteplase drotrecogin alfa ximelagatran Acquired factor VIII deficiency Desmoteplase Mitochondrial complex III deficiency Fluindione Antiplasmin deficiency Dysprothrombinemia, hereditary Owren disease Factor VII deficiency Factor X deficiency Carbohydrate-deficient glycoprotein syndrome type 1b Dabigatran etexilate Stauffer syndrome Factor XIII deficiency ancrod Fibrinolysin Anistreplase Reteplase plasminogen Anisindione tipranavir Congenital afibrinogenaemia Low molecular weight heparins Protamine sulfate Ardeparin.

Asparaginase asparaginase Asparaginase or Colaspase, the enzyme that catalyzes the hydrolysis of asparagine to aspartic acid wikipedia Kasabach-Merritt syndrome Kasabach-Merritt syndrome Kasabach-Merritt syndrome, also known as Hemangioma with thrombocytopenia, the rare disease, usually of infants, in which a vascular tumor leads to decreased platelet counts and sometimes other bleeding problems, which can be life-threatening wikipedia Haemorrhagic disease of the newborn Haemorrhagic disease of the newborn Haemorrhagic disease of the newborn, a coagulation disturbance in newborns due to vitamin K deficiency wikipedia Phenprocoumon Phenprocoumon Phenprocoumon, the long-acting oral anticoagulant drug, a derivative of coumarin wikipedia Acenocoumarol Acenocoumarol Acenocoumarol, an anticoagulant that functions as a vitamin K antagonist wikipedia Phenindione Phenindione Phenindione, the anticoagulant which functions as a Vitamin K antagonist wikipedia heparin Heparin, a highly sulfated glycosaminoglycan, widely used as an injectable anticoagulant, and has the highest negative charge density of any known biological molecule wikipedia Reye's syndrome Reye syndrome (a form of encephalopathy with fatty infiltration of the liver, characterized by brain edema and vomiting that may rapidly progress to seizures; coma; and death) wikipedia von Willebrand disease von Willebrand disease, a most common hereditary coagulation abnormality described in humans, although it, which can also be acquired as a result of other medical conditions wikipedia tissue plasminogen activator Tissue plasminogen activator, a serine protease normally found on the surface of endothelial cells of veins, capillaries, a pulmonary artery, heart, and uterus, and is secreted after vascular injury wikipedia Rivaroxaban Rivaroxaban, the oral anticoagulant invented and manufactured by Bayer; in a number of countries it is marketed as Xarelto wikipedia antithrombin Antithrombin, a small protein molecule that inactivates several enzymes of the coagulation system wikipedia fondaparinux Fondaparinux, the anticoagulant medication chemically related to low molecular weight heparins wikipedia streptokinase Streptokinase, the enzyme secreted by several species of streptococci that can bind and activate human plasminogen wikipedia Vitamin K deficiency Vitamin K deficiency, the form of avitaminosis resulting from insufficient vitamin K1 or vitamin K2 or both wikipedia Haemophilia B Haemophilia B, a blood clotting disorder caused by a mutation of the Factor IX gene, leading to a deficiency of Factor IX wikipedia argatroban Argatroban (a synthetic derivative of L-arginine with antithrombotic activity) wikipedia Lassa fever Lassa fever, an acute viral hemorrhagic fever first described in 1969 in the town of Lassa, Nigeria, located in the Yedseram river valley wikipedia urokinase Urokinase, also called urokinase-type Plasminogen Activator, a serine protease wikipedia Bivalirudin Bivalirudin, the specific and reversible direct thrombin inhibitor wikipedia Haemophilia C Haemophilia C, a mild form of haemophilia affecting both sexes wikipedia Lepirudin Lepirudin, the anticoagulant that functions as a direct thrombin inhibitor wikipedia dicoumarol Dicoumarol or dicumarol, the naturally occurring anticoagulant that functions as a functional vitamin K depleter wikipedia Haem arginate Hemin, the iron-containing porphyrin wikipedia Tenecteplase Tenecteplase, the enzyme used as a thrombolytic drug wikipedia drotrecogin alfa Drotrecogin alfa, the recombinant form of human activated protein C that has anti-thrombotic, anti-inflammatory, and profibrinolytic properties wikipedia ximelagatran Ximelagatran, the anticoagulant that has been investigated extensively as a replacement for warfarin that would overcome the problematic dietary, drug interaction, and monitoring issues associated with warfarin therapy wikipedia Acquired factor VIII deficiency Acquired factor VIII deficiency, the cause and medical concept with DiseasesDB code "30965" Desmoteplase Desmoteplase, the class and cause with Mesh code "C069588" and DiseasesDB code "34409" Mitochondrial complex III deficiency Mitochondrial complex III deficiency, the cause and medical condition with DiseasesDB code "34368" Fluindione Fluindione, the class and cause with Mesh code "C017673" and DiseasesDB code "34266" Antiplasmin deficiency Antiplasmin deficiency, the cause and medical concept with DiseasesDB code "33712" Dysprothrombinemia, hereditary Dysprothrombinemia, hereditary, the cause and medical condition with DiseasesDB code "31828" Owren disease Owren disease (a deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia) Factor VII deficiency Factor vii deficiency (an autosomal recessive characteristic or a coagulation disorder acquired in association with vitamin k deficiency) Factor X deficiency Factor X deficiency (blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired) Carbohydrate-deficient glycoprotein syndrome type 1b Carbohydrate-deficient glycoprotein syndrome type 1b, the cause and medical concept with DiseasesDB code "31335" Dabigatran etexilate Dabigatran etexilate, the class and cause with Mesh code "C453962" and DiseasesDB code "34566" Stauffer syndrome Stauffer syndrome, a constellation of signs and symptoms of liver dysfunction that arise due to presence of renal cell carcinoma but are not due to tumour inflitration into the liver and/or intrinsic liver disease; it is a paraneoplastic syndrome wikipedia Factor XIII deficiency Factor XIII deficiency may occur very rarely, and, which can cause a severe bleeding tendency wikipedia ancrod Ancrod, the defibrinogenating agent derived from the venom of the Malayan pit viper wikipedia Fibrinolysin Fibrinolysin, an enzyme derived from plasma of bovine origin or extracted from cultures of certain bacteria wikipedia Anistreplase Anistreplase, the thrombolytic drug wikipedia Reteplase plasminogen activator, tissue, the gene plasminogen Plasminogen (precursor of fibrinolysin (plasmin)) Anisindione Anisindione, the synthetic anticoagulant and an indanedione derivative wikipedia tipranavir Tipranavir, or tipranavir disodium, the nonpeptidic protease inhibitor manufactured by Boehringer-Ingelheim under the trade name Aptivus wikipedia Congenital afibrinogenaemia Congenital afibrinogenaemia, the cause and medical concept with DiseasesDB code "307" Low molecular weight heparins Low molecular weight heparins (heparin fractions with a molecular weight usually between 4000 and 6000 kD) Protamine sulfate Protamine sulfate (a heparin assay is a device used to determine the level of the anticoagulant heparin in the patient's circulation) Ardeparin Ardeparin, the drug and cause with Mesh code "C093450" and DiseasesDB code "30546.

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