Microangiopathic hemolytic anemia is seen in _____, HUS, and HELLP syndrome
_____ gene mutation present on chromosome 1q is the most common genetic mutation seen in autosomal-recessive hereditary spherocytosis
_____ gene mutation present on chromosome 8p is the most common genetic mutation seen in autosomal-dominant hereditary spherocytosis
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
_____ test will help in diagnosis of factor XIII deficiency
Hereditary stomatocytosis is caused by missense mutations in _____ or RhAG
_____ gene mutation present on chromosome 1q21 is the most common genetic mutation seen in autosomal-dominant hereditary elliptocytosis
Hemophilia (A, B, C) presents with _____ PT and increased PTT
In β-thalassemia major, α₄ tetramers result in _____ erythropoiesis and extravascular hemolysis
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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