Hemoglobin >_____ g/dL or Hematocrit >49% in men + bone marrow showing trilineage (or panmyelosis) growth +JAK2 mutation are major criteria for Polycythemia Vera
_____ is caused by an acquired defect in myeloid stem cells, resulting in absent GPI
_____ gene mutation present on chromosome 8p is the most common genetic mutation seen in autosomal-dominant hereditary spherocytosis
_____ test will help in diagnosis of factor XIII deficiency
_____ is associated with free light chain excretion in the urine, known as Bence Jones proteinuria
Hereditary stomatocytosis is caused by missense mutations in _____ or AEP
Hemophilia (A, B, C) presents with _____ PT and increased PTT
In -thalassemia major, 4 tetramers result in _____ erythropoiesis and extravascular hemolysis
_____ gene mutation present on chromosome 1q is the most common genetic mutation seen in autosomal-recessive hereditary spherocytosis
Microangiopathic hemolytic anemia is seen in _____, HUS, and HELLP syndrome
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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