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| ==Introduction== | | ==Introduction== |
| Haemorrhagic diseases can be categorised by two different causal mechanisms: | | Haemorrhagic diseases can be categorised by two different causal mechanisms: |
− | *Increased vessel fragility which leads to a non-thrombocytopenic [[Haemorrhage_-_Pathology#Purpura|purpura]]. | + | *Increased vessel fragility which leads to a non-thrombocytopenic [[Haemorrhage#Purpura|purpura]]. |
| *Inadequate haemostatic response. This may be caused by [[Platelet Abnormalities|platelet dysfunction or deficiency]], which leads to a primary or secondary thrombocytopenic purpura, or [[Coagulation Factor Deficiency|deficiencies/derangements of clotting factors]]. | | *Inadequate haemostatic response. This may be caused by [[Platelet Abnormalities|platelet dysfunction or deficiency]], which leads to a primary or secondary thrombocytopenic purpura, or [[Coagulation Factor Deficiency|deficiencies/derangements of clotting factors]]. |
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| Drug-induced and heavy metal damage to the vascular system does occur, although the mechanisms are not clearly understood. Examples include lead, bismuth, mercury, iodides, fluorides, chlorinated hydrocarbon pesticides and salicylates. | | Drug-induced and heavy metal damage to the vascular system does occur, although the mechanisms are not clearly understood. Examples include lead, bismuth, mercury, iodides, fluorides, chlorinated hydrocarbon pesticides and salicylates. |
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− | Vascular fragility can occur as a consequence of an underlying disease state, which is seen in [[Type III Hypersensitivity|allergy]] or anaphylactic reactions, connective tissue diseases such as Ehlers-Danlos syndrome in dogs, [[DM|diabetes mellitus]] and [[:Category:Antibody Mediated Autoimmune Diseases|antibody-antigen complex reactions]]. | + | Vascular fragility can occur as a consequence of an underlying disease state, which is seen in allergy or [[Type I Hypersensitivity|anaphylactic reactions]], connective tissue diseases such as Ehlers-Danlos syndrome in dogs, [[DM|diabetes mellitus]] and [[Type III Hypersensitivity|antibody-antigen complex reactions]]. |
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| ==Platelet dysfunction== | | ==Platelet dysfunction== |
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| ==Clotting Factor Abnormalities== | | ==Clotting Factor Abnormalities== |
| [[Coagulation Factor Deficiency|Deficiencies]] in clotting factors are often the result of congenital deficiency in one or more of the coagulation factors and can lead to ineffective blood clotting and development of a disease syndrome characterized by excessive bleeding - deficiencies are often detected following trauma or surgery. Occasionally bleeding may be spontaneous (e.g. into alimentary or urinary tracts). Deficiencies are often seen as familial inherited problems; [[Coagulation_Factor_Deficiency#Factor_VIII|Haemophilia (factor VIII deficiency)]] is probably the best understood condition. | | [[Coagulation Factor Deficiency|Deficiencies]] in clotting factors are often the result of congenital deficiency in one or more of the coagulation factors and can lead to ineffective blood clotting and development of a disease syndrome characterized by excessive bleeding - deficiencies are often detected following trauma or surgery. Occasionally bleeding may be spontaneous (e.g. into alimentary or urinary tracts). Deficiencies are often seen as familial inherited problems; [[Coagulation_Factor_Deficiency#Factor_VIII|Haemophilia (factor VIII deficiency)]] is probably the best understood condition. |
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| + | Other coagulation defects can be induced by disease processes such as [[Angiostrongylosis|angiostrongylosis]], vitamin K deficiency ([[Anticoagulant Rodenticide Toxicity|rodenticide poisoning]]) or disseminated intravascular coagulation ([[Disseminated Intravascular Coagulation|DIC]]) |
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| [[Category:Haemorrhagic Diseases|A]] | | [[Category:Haemorrhagic Diseases|A]] |
| [[Category:To Do - Blood]] | | [[Category:To Do - Blood]] |
| + | [[Category:Cardiology Section]] |