α-thalassemia due to a _____ gene deletion is characterized by formation of β4 tetramers, known as HbH
Megaloblastic anemia occurs due to delayed maturation of the _____ relative to the cytoplasm of precursor RBCs
β-thalassemia mutations in β-globin genes result in _____ or diminished (β+) production of the β-globin chain
A normal reticulocyte count is between _____ to 1.5%
The typical normal values for a WBC differential (per USMLE) are:Neutrophils (~ _____%)Lymphocytes (~ 30%)Monocytes (~ 6%)Eosinophils (~ 3%)Basophils (~ 1%)
_____ is important and the strongest predictor of prognosis for Hodgkin lymphoma (Hodgkin or non-Hodgkin)
Lymphomas are malignancies of _____ leukocytes, whereas Leukemias are malignancies of immature leukocytes
Diagnostic criteria for CMML includes persistent peripheral blood monocytosis ≥ _____ x 10⁹/L, with monocytes accounting for ≥ 10% of the WBC count.
_____ is an anemia due to decreased synthesis of globin chains
The _____ Coombs test adds anti-human globulin (Coombs reagent) to a sample of a patient's RBCs
Anemias: Classification and Approach
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Hemolytic Anemias
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Myeloproliferative Neoplasms
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Myelodysplastic Syndromes
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Acute Leukemias
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Chronic Leukemias
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Lymphomas and Lymphoid Neoplasms
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Plasma Cell Disorders
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Bleeding Disorders
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Thrombotic Disorders
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