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Pathology – Blood clotting, White and Red blood cells, Bone marrow.

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Answer
Hemophilia:   Excessive bleeding caused by hereditary lack of blood clotting factors (factor VIII orIX) necessary for blood clotting.  
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Purpura:   Multiple pinpoint hemorrhages and accumulation of blood under the skin. ((Hemorrhages in the skin and mucous membrane crews red purple discoloration of the skin.)  
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Leukemia:   Increase in cancerous white blood cells (leukocytes).  
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Acute myelogenous leukemia:   Immature granulocytes (myeloblasts) leukemia (AML) predominate.  
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Acute lymphatic leukemia (ALL):   Immature lymphocytes (lymphoblasts) predominate. This form is seen most often in children and adolescents onset is sudden.  
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Chronic myelogenous (myelocytic) leukemia (CML):   Both mature and immature granulocytes are present in large numbers in the marrow in the blood.  
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Chronic lymphocytic leukemia (CLL):   Abnormal numbers of relatively mature lymphocytes predominate in the marrow, Nick knows and spleen.  
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Mononucleosis:   Infectious disease marked by increased numbers of mononuclear leukocytes in a large cervical lymph nodes. (This disease is transmitted by the Epstein-Barr virus (EBV).  
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Multiple myeloma:   Malignant neoplasm of bone marrow.  
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Anemia:   Efficiency in erythrocyte or hemoglobin.  
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Aplastic anemia:   Failure of blood cell production in the bone marrow.  
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Hemolytic anemia:   Reduction in blood cells due to excessive destruction.  
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Pernicious anemia:   Lack of mature erythrocytes caused by an inability to explore vitamin B12 into the bloodstream.  
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Sickle cell anemia:   Hereditary disorder of abnormal hemoglobin producing sickle – shaped erythrocyte and hemolysis.  
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Thalassemia:   Inherited defects in ability to produce hemoglobin leading to hypochromia.  
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Hemochromatosis:   Excess iron deposits throughout the body.  
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Polycythemia vera:   General increase in red blood cells (erythremia).  
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