Match the LD isoenzyme on the left with the corresponding disorder on the right. LD-1 LD-2 LD-3 LD-4 LD-5 Megaloblastic Anemia Myocardial Infarction Pulmonary Embolism carcinoma Hepatic Injury
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- Divide each term into its component word parts. Write these word parts, in sequence, on the lines provided. When necessary use a slash/ to indicate a combining vowel. You may not need all of the lines provided. Aplastic anemia is characterized by an absence of all formed blood elements. ________________ _________________ ________________ ________________Thrombocytopenia (throm-bo-sye-tow-pee-ne-ah) is a disorder that develops when certain drugs, bone marrow cancer, or radiation destroys red bone marrow, including stem cells that give rise to platelets. Predict a likely symptom of this disorder.Which LDH isoenzyme is elevated in myocardial infarction? Explain why. What LDH isoenzyme can be use as a liver function test? Explain why.
- The hyperviscosity shndrome can cause cardiac ischemia by impairing micro circulation and this syndrome is associated with erythrocytosis, leukocytes is, or hypercholesterolemi. For each condition provide a definition, indicate two causes for each condition and give the normal values.Provide the expected result of clotting time if the patient is afflicted with the following condition. P if Prolonged and N if Normal. 1.1 Vascular Disorder 1.2 Fibrinogen Deficiency 1.3 Prothrombin Deficiency 1.4 Factor VII Deficiency 1.5 Classic HemophiliaA patient most likely presents with chronic myeloid leukemia (CML) and you have a full blood cell count (CBC) preformed. Which CBC profile most likely matches a CML diagnosis? Normal CBC ranges: Hb 115-175 g/L; WBC 4-11 x 10/L; platelets 150- 400 x 10/L. O Hb 82 g/L, WBC 175 x 10/L; platelets 115 x 10/L. O Hb 60 g/L, WBC 12 x 10/L; platelets 420 x 10/L. O Hb 250 g/L, WBC 25 x 10/L; platelets 650 x 10/L. O Hb 160 g/L, WBC 10 x 10/L platelets 500 x 10/L. Hb 130 g/L WBC 6 x 10/L platelets 500 x 10/L
- A female 40 year old patient has a hematocrit of 60%, an elevated reticulocyte count, and splenomegaly. What is a possible condition this patient has? O chronic myelogenous leukemia O lymphoma O aplastic anemia O pernicious anemia O polycythemia O thrombocytopenia O septicemiaA 67-year-old woman complains of gradually increasing fatigue. On physical examination, she is found to be anemic and has a peripheral neuropathy characterized by loss of position and vibratory sense. Laboratory studies docu- ment a macrocytic anemia and decreased WBC and platelets counts. What pathological mechanism accounts for these findings? Myelodysplastic sideroblastic anemia Chronic blood loss Autoantibodies against parietal cells or intrinsic factor Diabetes mellitus A diet deficient in folateIDENTIFY THE TYPE OF BLEEDING THAT IS ASSOCIATED WITH THE FF. COAGULATION FACTOR DEFICIENCY. CHOOSE THE ANSWER FROM THE BOX BELOW. TYPE OF BLEEDING COAGULATION FACTOR DEFICIENCY FII, VIII, FIX FII, VIII, FIX, FXI FVIIII, FIX,FX Fibrinogen, FII,FV,FVII,FVIII, FIX, FX,FXI,FXII FVII,FVIII,FIX,FXIII Fibrinogen, FXIII FX, FXIII Fibrinogen, FXIII Abnormal fibrinogen FXII, prekallikrein, high molecular weight kininogen Easy Bruising Asymptomatic Hematomas Mucosal bleeding Intracranial bleeding Miscarriage Thrombosis Hemarthrosis Umbilical cord bleeding Postsurgical bleeding Delayed wound healing
- Cite one blood disorder following the condition as stated in the first column and discuss each in 2-3 sentences. Name the blood disorder and discuss each in 2-3 sentences. Blood disorder affecting Red Blood Cells Blood disorder affecting White Blood Cells Blood disorder affecting Platelets Blood disorder affecting Blood PlasmaElsa’s pediatrician suspects that she has thalassemia. Which of the following statements is true of thalassemia? Thrombocytes tend to “stick together” and form blood clots. Thalassemia is always caused by diet and environmental factors, not genetic makeup. Thalassemia is also known as erythroblastic anemia and involves a reduced amount of hemoglobin in the blood. Thalassemia is a type of hemophilia and is often hereditary in females.