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Diseases of the blood (hematology)

Hemoglobin S-C disease: causes, symptoms, diagnosis, treatment

Hemoglobin S-C disease is hemoglobinopathy, the symptom of which is similar to that of sickle-cell anemia, but less intense.

Hemoglobin C: Causes, Symptoms, Diagnosis, Treatment

Hemoglobin C disease is hemoglobinopathy, the symptom of which is similar to that of sickle-cell anemia, but less intense.

Sickle-cell anemia: causes, symptoms, diagnosis, treatment

Sickle-cell anemia (hemoglobinopathy) is a chronic hemolytic anemia, occurring predominantly in blacks in America and Africa, due to homozygous inheritance of HbS

Deficiency of glucose-6-phosphate dehydrogenase (G6FD): causes, symptoms, diagnosis, treatment

Deficiency of glucose-6-phosphate dehydrogenase (G6PD) is X-linked fermentopathy, is more common in people of negroid race, hemolysis can occur after acute illness or intake of oxidants (including salicylates and sulfonamides).

Deficiency of glycolic enzymes in Embden-Meyerhof: causes, symptoms, diagnosis, treatment

Deficiency of enzymes glybolysis Embden-Meyerhofa - a rare autosomal recessive metabolic disease of erythrocytes, causing hemolytic anemia.

Stomatocytosis and anemia developing with hypophosphatemia: causes, symptoms, diagnosis, treatment

Stomatocytosis (the presence of cup-shaped concave erythrocyte form) and anemia that develops during hypophosphatemia are abnormalities of the erythrocyte membrane causing hemolytic anemia

Hereditary Spherocytosis and Hereditary Elliptocytosis: Causes, Symptoms, Diagnosis, Treatment

Hereditary spherocytosis and hereditary elliptocytosis are congenital anomalies of the erythrocyte membrane. With hereditary spherocytosis and elliptocytosis, the symptoms are usually mild and include anemia of varying severity, jaundice and splenomegaly.

Hemolytic anemia associated with mechanical damage of erythrocytes

Hemolytic anemia associated with mechanical damage to erythrocytes (microangiopathic hemolytic anemia) is caused by intravascular hemolysis as a result of intensive trauma or with turbulence of the blood flow.

Paroxysmal nocturnal hemoglobinuria (Marciafawa-Mikeli syndrome): causes, symptoms, diagnosis, treatment

Paroxysmal nocturnal hemoglobinuria (Markiafawa-Mikeli syndrome) is a rare disease characterized by intravascular hemolysis and hemoglobinuria and worsening during sleep.

Autoimmune hemolytic anemia

Autoimmune hemolytic anemia is caused by antibodies that interact with erythrocytes at a temperature of 37 ° C (hemolytic anemia with thermal antibodies) or a temperature of <37 ° C (hemolytic anemia with Cold agglutinins).

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