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BOC HEMATOLOGY EXAM 1 QUESTIONS WITH VERIFIED ANSWERS [ GRADED A+]

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BOC HEMATOLOGY EXAM 1 QUESTIONS WITH VERIFIED ANSWERS [ GRADED A+] Megaloblastic asynchronous development in the bone marrow indicates which one of the following? - impaired synthesis of DNA Which of the following are found in association with megaloblastic anemia? - neutropenia and thrombocytopenia Which of the following represents characteristic features of iron metabolism in patients with anemia of chronic disease? Serun iron Transferrin saturation TIBC result A normal normal normal result B increased increased nor/sl inc result C normal marked inc normal ©morren2024/2025.Year published 2024. result D decreased decreased nor/decre - result d A characteristic morphologic feature in hemoglobin C disease is: - target cells Thalassemias are characterized by: - decreased rate of globin synthesis A patient has the following blood values: RBC 6.5 Hgb: 13.0 Hct: 39.0% MCV: 65 MCH: 21.5 MCHC: 33% These results are compatible with: - Thalassemia minor ©morren2024/2025.Year published 2024.

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BOC HEMATOLOGY EXAM 1 QUESTIONS

WITH VERIFIED ANSWERS [ GRADED A+]




Megaloblastic asynchronous development in the bone marrow indicates which

one of the following? - ✔✔impaired synthesis of DNA




Which of the following are found in association with megaloblastic anemia? -

✔✔neutropenia and thrombocytopenia




Which of the following represents characteristic features of iron metabolism in

patients with anemia of chronic disease? Serun iron Transferrin saturation TIBC


result A normal normal normal


result B increased increased nor/sl inc


result C normal marked inc normal


©morren2024/2025.Year published 2024.

, result D decreased decreased nor/decre - ✔✔result d




A characteristic morphologic feature in hemoglobin C disease is: - ✔✔target cells




Thalassemias are characterized by: - ✔✔decreased rate of globin synthesis




A patient has the following blood values:


RBC 6.5


Hgb: 13.0


Hct: 39.0%


MCV: 65


MCH: 21.5


MCHC: 33%


These results are compatible with: - ✔✔Thalassemia minor




©morren2024/2025.Year published 2024.

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