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  2. Heinz body - Wikipedia

    en.wikipedia.org/wiki/Heinz_body

    The presence of Heinz bodies represents damage to hemoglobin and is classically observed in G6PD deficiency, a genetic disorder that causes hemolytic anemia. In veterinary medicine, Heinz bodies may be seen following the consumption of foods containing thiosulfate and propylene glycol compounds by cats, dogs and certain primates.

  3. Glucose-6-phosphate dehydrogenase deficiency - Wikipedia

    en.wikipedia.org/wiki/Glucose-6-phosphate_de...

    Most individuals with G6PD deficiency are asymptomatic.When it induces hemolysis, the effect is usually short-lived. [5]Most people who develop symptoms are male, due to the X-linked pattern of inheritance, but female carriers can be affected due to unfavorable lyonization or skewed X-inactivation, where random inactivation of an X-chromosome in certain cells creates a population of G6PD ...

  4. Degmacyte - Wikipedia

    en.wikipedia.org/wiki/Degmacyte

    A degmacyte or bite cell is an abnormally shaped mature red blood cell with one or more semicircular portions removed from the cell margin, known as "bites". [1] [2] These "bites" result from the mechanical removal of denatured hemoglobin during splenic filtration as red cells attempt to migrate through endothelial slits from splenic cords into the splenic sinuses. [3]

  5. Coombs test - Wikipedia

    en.wikipedia.org/wiki/Coombs_test

    ABO hemolytic disease of the newborn (the direct Coombs test may only be weakly positive) Anti-Kell hemolytic disease of the newborn; Rh c hemolytic disease of the newborn; Rh E hemolytic disease of the newborn; Other blood group incompatibility (RhC, Rhe, Kidd, Duffy, Lewis, MN, P and others) Alloimmune hemolytic transfusion reactions

  6. Pyruvate kinase deficiency - Wikipedia

    en.wikipedia.org/wiki/Pyruvate_kinase_deficiency

    Pyruvate kinase deficiency is an inherited metabolic disorder of the enzyme pyruvate kinase which affects the survival of red blood cells. [4] [5] Both autosomal dominant and recessive inheritance have been observed with the disorder; classically, and more commonly, the inheritance is autosomal recessive.

  7. List of hematologic conditions - Wikipedia

    en.wikipedia.org/wiki/List_of_hematologic_conditions

    Autoimmune hemolytic anemia: D59.0-D59.1: Autoimmune hemolytic anemia (AIHA) is a type of hemolytic anemia where the body's immune system attacks its own red blood cells (RBCs), leading to their destruction . [28] [29] Types of AIHA include warm autoimmune hemolytic anemia, cold agglutinin disease, and paroxysmal cold hemoglobinuria.

  8. Basophilic stippling - Wikipedia

    en.wikipedia.org/wiki/Basophilic_stippling

    Blood smear showing red blood cells with basophilic stippling. Basophilic stippling, also known as punctate basophilia, is the presence of numerous basophilic granules that are dispersed through the cytoplasm of erythrocytes in a peripheral blood smear.

  9. Drug-induced nonautoimmune hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Drug-induced_nonautoimmune...

    These Heinz bodies are then removed by macrophages in the spleen, causing hemolysis and forming bite cells. [14] Hemolytic anemia can also occur in drug-induced thrombotic microangiopathies (DITMA) where drugs cause platelets to collect together to form platelet collections against the walls of the small vessels of the body. These collections ...