Match the microcytic anemia with the cause of the anemia. Question 8 options: 12345 Sideroblastic anemia...
Match the microcytic anemia with the cause of the anemia.
Question 8 options:
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Homework Answers
Answers:
1.Sideroblastic anemia - Defective incorporation of iron into the hemoglobin molecule
2. Iron deficiency anemia - Chronic GI bleeder
3. Haemoglobin EE disease - Abnormal production of the globin chain of hemoglobin
4. Thalassemia - Decrease in the production of one of the globin chains
5. Anemia of chronic disease - Iron is trapped in the macrophages & is unavailable to the RBCs.
Add Answer to:
Match the microcytic anemia with the cause of the anemia.
Question 8 options:
12345
Sideroblastic anemia...
match the conditions and the pathogenic mechanisms Temporary suppression of erythropoiesis following a viral infection (often...
match the conditions and the pathogenic mechanisms
Temporary suppression of erythropoiesis following a viral infection (often a Parvovirus B19 infection in a child) Choose Aplastic anemia resulting from defects in DNA repair mechanisms resulting in increased rates of apoptosis and ineffective erythropoiesis Choose... Sickle Cell Anemia Lack of sufficient iron stores to support erythropoiesis Anemia of Chronic Disease Congenital pure red cell aplasia; likely the result of a failure of red cell progenitors to respond to erythropoietic cytokines Fanconi Anemia...
Please check if my answers are correct Temporary suppression of erythropoiesis following a viral infection (often...
Please check if my answers are correct
Temporary suppression of erythropoiesis following a viral infection (often a Parvovirus B19 infection in a child) Transient Erythroblastopenia of Childhood - Aplastic anemia resulting from defects in DNA repair mechanisms resulting in increased rates of apoptosis and ineffective erythropoiesis Fanconi Anemia Lack of sufficient iron stores to support erythropoiesis Iron Deficiency Anemia Congenital pure red cell aplasia; likely the result of a failure of red cell progenitors to respond to erythropoietic cytokines Diamond-Blackfan...
Temporary suppression of erythropoiesis following a viral infection (often a Parvovirus B19 infection in a child)...
Temporary suppression of erythropoiesis following a viral infection (often a Parvovirus B19 infection in a child) Choose Aplastic anemia resulting from defects in DNA repair mechanisms resulting in increased rates of apoptosis and ineffective erythropoiesis Choose... Sickle Cell Anemia Lack of sufficient iron stores to support erythropoiesis Anemia of Chronic Disease Congenital pure red cell aplasia; likely the result of a failure of red cell progenitors to respond to erythropoietic cytokines Fanconi Anemia Extrinsic Hemolytic Anemia Intravascular or extravascular destruction...
Compare and contrast the causes and consequences and diagnostic indicators of microcytic and macrocytic anaemias. (Please...
Compare and contrast the causes and consequences and diagnostic indicators of microcytic and macrocytic anaemias. (Please could you answer the question in details) I've started it but I need to go in depth . Thanks Microcytic anaemia occurs when the size of the RBC is small (the MCV is low <83fl), whereas macrocytic anaemia is when the size of the RBC is large (the MCV is high >101fl). Microcytic anaemia usually results from processes that impair haemoglobin synthesis in the...
PLEASEEE ANSWER ALL OF THESE QUESTIONS ANSWER FAST 13. Which of these statements is INCORRECT about...
PLEASEEE ANSWER ALL OF THESE QUESTIONS ANSWER FAST
13. Which of these statements is INCORRECT about pre-hepatic jaundice An increase of unconjugated bilirubin levels in the blood b. Could be cause by Criggler-Najjar syndrome c. There is an increase in hemoglobin breakdown producing large amount of bilirubin a. d. Could lead to kernicterus in newborn 14. Correct statement about hepatitis A infection: a. Spreads from one person to another via body fluids (saliva, semen, blood b, c Occurs only with...
complete the anemia chart as you study each anemia. Try to visualize a microscopic field that...
complete the anemia chart as you study each anemia. Try to
visualize a microscopic field that represents each of the anemias.
list the three distinguishing characteristic of each anemia. This
chart can be used to organize the theory to study the
anemia
Do what you ean, this is meant to PARTI - Anemias I help you study! Comprehensive Anemia Chart Worth 6 points 49 Ask students to complete the chart, noting key facts for each anemia in the sequence studied....
Match the following conditions with their definitions below: aplastic anemia mononucleosis sickle cell anemia hemochromatosis thalassemia...
Match the following conditions with their definitions below: aplastic anemia mononucleosis sickle cell anemia hemochromatosis thalassemia hemolytic anemia polycythemia vera hemophilia purpura 1. General increase in red blood cells (erythremia). 2. Excess iron deposits throughout the body 3. Hereditary condition characterized by abnormal crescent shape of erythrocytes and by destruction of red blood cells 4. Inherited defect in the ability to produce hemoglobin, usually seen in persons of Mediterranean background 5. Infectious disease marked by increased numbers of leukocytes and...
this is a review ungraded assignment please help me to understand the answers Megaloblastic Anemias due...
this is a review ungraded assignment please help me to
understand the answers
Megaloblastic Anemias due to cobalamin deficiency are most often caused by: Select one: a. Decreased dietary intake of Vitamin B12 o b. Drug inhibition O c. Lack of intrinsic factor O d. Increased requirements O CIFAR MV CHOICE Match the following globin chain pairings to the appropriate hemoglobin type: a2B2 Choose... 4282 Choose... d2Y2 Choose... < PREVIOUS NEXT Σ. Choose... Hemoglobin A Hemoglobin F Hemoglobin A2 Match...
Case 8 Hemoglobin, the Oxygen Carrier Focus concept A mutation in the gene for hemoglobin results...
Case 8 Hemoglobin, the Oxygen Carrier Focus concept A mutation in the gene for hemoglobin results in an altered protein responsible for the disease sickle cell anemia. An understanding of the biochemistry of the disease may suggest possible treatments Prerequisite Hemoglobin structure and function concepts Background Normal adult hemoglobin is called Hemoglobin A (Hb A). Ninety-eight percent ofaduk hemoglobin is Hb A and 2% is Hb A. There are other forms of hemoglobin. For example, the deve loping fetus has...
Please check if my answers are correct this is reciew assignment Megaloblastic Anemias due to cobalamin...
Please check if my answers are correct this is reciew
assignment
Megaloblastic Anemias due to cobalamin deficiency are most often caused by: Select one: • a. Decreased dietary intake of Vitamin B12 O b. Drug inhibition O c. Lack of intrinsic factor Od. Increased requirements Clear my choice Match the following globin chain pairings to the appropriate hemoglobin type: C2B2 Hemoglobin A . 0262 Hemoglobin A2 = AzY2 Hemoglobin F. 4 Match the following biochemical pathways with their role in...
match the conditions and the pathogenic mechanisms
Temporary suppression of erythropoiesis following a viral infection (often a Parvovirus B19 infection in a child) Choose Aplastic anemia resulting from defects in DNA repair mechanisms resulting in increased rates of apoptosis and ineffective erythropoiesis Choose... Sickle Cell Anemia Lack of sufficient iron stores to support erythropoiesis Anemia of Chronic Disease Congenital pure red cell aplasia; likely the result of a failure of red cell progenitors to respond to erythropoietic cytokines Fanconi Anemia...
Please check if my answers are correct
Temporary suppression of erythropoiesis following a viral infection (often a Parvovirus B19 infection in a child) Transient Erythroblastopenia of Childhood - Aplastic anemia resulting from defects in DNA repair mechanisms resulting in increased rates of apoptosis and ineffective erythropoiesis Fanconi Anemia Lack of sufficient iron stores to support erythropoiesis Iron Deficiency Anemia Congenital pure red cell aplasia; likely the result of a failure of red cell progenitors to respond to erythropoietic cytokines Diamond-Blackfan...
Temporary suppression of erythropoiesis following a viral infection (often a Parvovirus B19 infection in a child) Choose Aplastic anemia resulting from defects in DNA repair mechanisms resulting in increased rates of apoptosis and ineffective erythropoiesis Choose... Sickle Cell Anemia Lack of sufficient iron stores to support erythropoiesis Anemia of Chronic Disease Congenital pure red cell aplasia; likely the result of a failure of red cell progenitors to respond to erythropoietic cytokines Fanconi Anemia Extrinsic Hemolytic Anemia Intravascular or extravascular destruction...
PLEASEEE ANSWER ALL OF THESE QUESTIONS ANSWER FAST
13. Which of these statements is INCORRECT about pre-hepatic jaundice An increase of unconjugated bilirubin levels in the blood b. Could be cause by Criggler-Najjar syndrome c. There is an increase in hemoglobin breakdown producing large amount of bilirubin a. d. Could lead to kernicterus in newborn 14. Correct statement about hepatitis A infection: a. Spreads from one person to another via body fluids (saliva, semen, blood b, c Occurs only with...
complete the anemia chart as you study each anemia. Try to
visualize a microscopic field that represents each of the anemias.
list the three distinguishing characteristic of each anemia. This
chart can be used to organize the theory to study the
anemia
Do what you ean, this is meant to PARTI - Anemias I help you study! Comprehensive Anemia Chart Worth 6 points 49 Ask students to complete the chart, noting key facts for each anemia in the sequence studied....
Match the following conditions with their definitions below: aplastic anemia mononucleosis sickle cell anemia hemochromatosis thalassemia hemolytic anemia polycythemia vera hemophilia purpura 1. General increase in red blood cells (erythremia). 2. Excess iron deposits throughout the body 3. Hereditary condition characterized by abnormal crescent shape of erythrocytes and by destruction of red blood cells 4. Inherited defect in the ability to produce hemoglobin, usually seen in persons of Mediterranean background 5. Infectious disease marked by increased numbers of leukocytes and...
this is a review ungraded assignment please help me to
understand the answers
Megaloblastic Anemias due to cobalamin deficiency are most often caused by: Select one: a. Decreased dietary intake of Vitamin B12 o b. Drug inhibition O c. Lack of intrinsic factor O d. Increased requirements O CIFAR MV CHOICE Match the following globin chain pairings to the appropriate hemoglobin type: a2B2 Choose... 4282 Choose... d2Y2 Choose... < PREVIOUS NEXT Σ. Choose... Hemoglobin A Hemoglobin F Hemoglobin A2 Match...
Case 8 Hemoglobin, the Oxygen Carrier Focus concept A mutation in the gene for hemoglobin results in an altered protein responsible for the disease sickle cell anemia. An understanding of the biochemistry of the disease may suggest possible treatments Prerequisite Hemoglobin structure and function concepts Background Normal adult hemoglobin is called Hemoglobin A (Hb A). Ninety-eight percent ofaduk hemoglobin is Hb A and 2% is Hb A. There are other forms of hemoglobin. For example, the deve loping fetus has...
Please check if my answers are correct this is reciew
assignment
Megaloblastic Anemias due to cobalamin deficiency are most often caused by: Select one: • a. Decreased dietary intake of Vitamin B12 O b. Drug inhibition O c. Lack of intrinsic factor Od. Increased requirements Clear my choice Match the following globin chain pairings to the appropriate hemoglobin type: C2B2 Hemoglobin A . 0262 Hemoglobin A2 = AzY2 Hemoglobin F. 4 Match the following biochemical pathways with their role in...
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