Registry study questions
Hemoglobin
Hemosiderin
Myoglobin
Transferrin
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Shorten the replication time of the granulocytes
Stimulate RNA syntheses of erythroid cells
Increase colony-stimulating factors produced by the B-lymphocytes
Decrease the release of marrow reticulocytes
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Osmotic fragility
Sucrose hemolysis
Heat instability test
Kleinhauer-Betke
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Macrocytosis
Target cells (codocytes)
Basophilic stippling
Rouleaux formation
A microscope adjustment
Immature cell forms in the peripheral blood
A trend on a Levy-Jennings chart
A calibration adjustment on an instrument
Complexed with haptoglobin
Freely circulating in the cytoplasm
Attached to transferrin
In the ferrous state
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Teardrop cells
Target cells
Spherocytes
Sickle cells
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Iron
Vitamin B12
Folic acid
Erythropoietin
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Iron, porphyrin, and amino acids
Iron, protoporphyrin, and globin
Heme, protoporphyrin, and amino acids
Heme, hemosiderin, and globin
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Rubricytes (polychromatophilic normoblast)
Reticulocytes
Sickle cells
Target cells
Elevated
Normal
Decreased
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Regulate the level of 2,3-DPG
Provide reduced glutathione to prevent oxidation of hemoglobin
Prevent the reduction of heme iron
Provide energy for membrane maintenance
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Storage of red blood cells
Production of red blood cells
Synthesis of erythropoietin
Removal of imperfect and aging cells
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Lactate dehydrogenase deficiency
G-6-PD deficiency
Pyruvate kinase deficiency
Hexokinase deficiency
Remaining RNA in the cell
Iron before it precipitates
Cell membrance before it dries out
Denatured hemoglobin in the cell
Pancytopenia and macrocytosis
Leukocytosis and elliptocytosis
Leukocytosis and ovalocytosis
Pancytopenia and microcytosis
Readily identified with polychrome stains
Rarely found in glucose-6-phosphate dehydrogenase deficient erythrocytes
Closely associated with spherocytes
Denatured hemoglobin inclusions that are readily removed by the spleen
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Ribosome
Chromatin
Mitochondria
Golgi area
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A
B
C
D
Temperature-dependent
Complement-independent
Antibody-mediated
Caused by a red cell membrane defect
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Erythrocytes
Granulocytes
Lymphocytes
Thrombocytes
Normal or slightly increased erythrocyte survival; normal osmotic fragility
Decreased erythrocyte survival; increased catabolism of heme
Decreased serum lactate dehydrogenase activity; normal catabolish of heme
Normal concentration of haptoglobin; marked hemoglobinuria
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Erythrocytes
Granulocytes
Lymphocytes
Thrombocytes
Autosomal dominant inheritance
Red cell membrane defects
Positive DAT
Measured platelet count
Iron deficiency anemia
Anemia of chronic inflammation
Hemochromatosis
Acute blood loss
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Reticulocyte count
Platelet factor 3
Serum B12 and folate
Leukocyte alkaline phosphatase
Macrocytosis
Target cells
Basophilis stippling
Rouleaux formation
4,3,1,2
2,3,1,4
4,2,3,1
2,1,3,4
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Microcytic, hypochromic
Macrocytic, hypochromic
Normocytic, normochromic
Microcytic, normochromic
Wright
Prussian blue
Crystal violet
Periodic acid-Schiff
Normal
High
Low
Variable
Hemolytic anemia
Multiple myeloma
G-6-PD deficiency
Myeloid metaplasia
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Retic count
Sedimentation rate
Hematocrit
Erythrocyte count
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Congenital hemolytic spherocytosis
March hemoglobinuria
Acquired hemolytic anemia
Thalassemia major
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Persistently increased M:E ratio
Megaloblastoid erythropoiesis
Marked thrombocytosis
Decreased ferritin levels
Spherocyte
Leptocyte
Microcyte
Macrocyte
Polycythemia vera
Systemic lupus erythematosus
Iron deficiency anemia
Hemoglobin SC disease
Proliferation of erythrocyte precursors
Impaired synthesis of DNA
Inadequate production of erythropoietin
Deficiency of G-6-PD
Neutropenia and thrombocytopenia
Decreased LD activity
Increased erythrocyte folate levels
Decreased plasma bilirubin levels
Congenital ovalocytosis
Hemoglobin C disease
Poor RBC fixation
Delay in smear preparation
Marrow hypoplasia
Inadequate erythropoiesis
Vitamin B12 deficiency
Increased erythropoietin production
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