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ASCP HEMATOLOGY EXAM-MLT Questions and Answers Latest Versions 2025 GRADED A+.

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ASCP HEMATOLOGY EXAM-MLT Questions and Answers Latest Versions 2025 GRADED A+.

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ASCP HEMATOLOGY










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ASCP HEMATOLOGY
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ASCP HEMATOLOGY EXAM-MLT Questions
and Answers Latest Versions 2025 GRADED
A+

Patients with A(-) type G-6-PD deficiency are least likely to
have hemolytic episodes in which of the following situations?


A. following administration of oxidizing drugs
B. following ingestion of fava beans
C. during infections
D. spontaneously correct answerD. spontaneously


A patient has a congenital nonspherocytic hemolytic anemia.
After exposure to anti-malarial drugs, the patient experiences
a severe hemolytic episode. This episode is characterized by
red cell inclusions caused by hemoglobin denaturation. Which
of the following conditions is most consistent with these
findings?


A. G-6-PD deficiency
B. thalassemia major

,C. pyruvate kinase deficiency
D. paroxysmal nocturnal hemoglobinuria correct answerA. G-
6-PD deficiency


Peripheral blood smears from patients with untreated
pernicious anemia are characterized by:


A. pancytopenia and macrocytosis
B. leukocytosis and elliptocytosis
C. leukocytosis and ovalocytosis
D. pancytopenia and microcytosis correct answerA.
pancytopenia and macrocytosis


Laboratory tests performed on a patient indicate
macrocytosis, anemia, leukopenia, and thrombocytopenia.
Which of the following disorders is the patient most likely to
have?


A. anemia of chronic disorder
B. vitamin B12 deficiency
C. iron deficiency
D. acute hemorrhage correct answerB. vitamin B12 deficiency

, The characteristic morphological feature in folic acid
deficiency is:


A. macrocytosis
B. target cells
C. basophilic stippling
D. rouleax formation correct answerA. macrocytosis


The most likely cause of the macrocytosis that often
accompanies anemia of myelofibrosis is:


A. folic acid deficiency
B. increased reticulocyte count
C. inadequate B12 absorption
D. pyroxine deficiency correct answerA. folic acid deficiency


A characteristic morphologic feature in hemoglobin C disease
is:


A. macrocytosis

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