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[DOC File]HEMOPHILIA
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impaired body's ability to control blood clotting or coagulation. lifelong condition with no cure (other than liver transplantation. Causes. Hemophilia A is an X-linked genetic disorder involving a lack of functional clotting Factor VIII and represents 90% of hemophilia cases
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[DOC File]Lecture: Physiology of Blood
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2. Polycythemia - excess RBC count, causes thick blood. a. polycythemia vera - bone marrow problem; hematocrit may jump to 80%. b. secondary polycythemia - high altitude (normal); or too much erythropoietin release. c. blood doping in athletes - RBCs previously withdrawn are transfused before an event; more RBCs, more oxygen delivery to the ...
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[DOCX File]Blood - Georgia Highlands College
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Blood. 1. Functions. A) Transportation of nutrients & waste. ... Primary polycythemia (polycythemia vera) b) Secondary polycythemia. FYI: Blood-doping. ... Leukocytic Disorders. 1) Leukopenia – decreased WBC count. a) Often caused by gluccocorticoids and various cancer & …
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[DOCX File]Blood - Georgia Highlands College
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Blood. 1. Functions. A) Transportation of . B) Regulation of . C) Protection from . 2. Characteristics ... Primary polycythemia (polycythemia vera) b) Secondary polycythemia. FYI: Blood-doping. ... Leukocytic Disorders. 1) Leukopenia – decreased WBC count. a) Often caused by gluccocorticoids and various cancer & HIV drugs ...
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[DOC File]HEMATOLOGY LECTURE NOTES
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Metabolic disorders e.g. diabetic ketoacidosis, uremia, and eclampsia. Steroid therapy. Acute hemorrhage or hemolysis. Changes in neutrophil morphology in disease states include: Left shift - this is the appearance in the peripheral blood of more immature components of the maturation pool. Dohle bodies and cytoplasmic vacuolation
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[DOC File]Circulatory System Research Project
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Hypercoagulable Disorders . Thrombosis. Factor I deficiency Hemophilia A or B You may research a disorder not listed above but this disease / disorder must deal with bleeding problems (either excessive clotting or lack of clotting) Blood disorders-- Aplastic Anemia. Polycythemia. Acute Leukemia. Physiologic jaundice. Thalassemia . Sickle cell ...
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[DOC File]The Hemic and Lymphatic Systems - Veterans Affairs
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Myeloproliferative Disorders: (Diagnostic Codes 7704, 7718, 7719). 7704 Polycythemia vera: Requiring peripheral blood or bone marrow stem-cell transplant or chemotherapy (including myelosuppressants) for the purpose of ameliorating the symptom burden. 100 Requiring phlebotomy 6 or more times per 12-month period or molecularly targeted therapy ...
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[DOC File]M29-1, Part 5, S - Veterans Affairs
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Its functions are many and varied. The spleen may become involved secondarily in any number of diseases, most of which result in varying degrees of splendic enlargement (splenomegaly), such as Banti's disease, blood disorders, malignancy, portal cirrhosis, tuberculosis, syphilis, and chronic malaria.
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[DOC File]POLYCYTHEMIA
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Increased blood volume and viscosity – interferes with cardiac output. Hypertension is common. Thromboembolism – 15 – 60% in those with PV (Gaspard, 2005). Rarely malignant. Hallmark of polycythemia is an elevated hematocrit >55%. CMPD’s include PV, idiopathic myelofibrosis, and essential throbocytosis, CML. Secondary polycythemia
is polycythemia considered cancer

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Red blood cells disorders . Mosab Nouraldein Mohammed Hamad . Faculty of health sciences, Elsheikh Abdallah Elbadri University, Sudan ... Polycythemia vera. 41. Morphological abnormalities of red ...
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Blood disorders polycythemia