
Congenital Sideroblastic Anemia Due to HSPA9 Gene Mutation
A clinical case of congenital sideroblastic anemia with HSPA9 mutation: blood picture, dyserythropoiesis, and ring sideroblasts in bone marrow.
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A clinical case of congenital sideroblastic anemia with HSPA9 mutation: blood picture, dyserythropoiesis, and ring sideroblasts in bone marrow.

How iron deficiency anemia was described in the 16th century: chlorosis, maiden's disease, and the first clinical observations by German physician Johannes Lange.

A clinical case of macrophages found in the urine sediment of a child with hemolytic anemia. Microscopy of native preparation and erythrocyte detritus.

Comparative table of myelogram changes in anemias, infections, leukemias, and agranulocytosis, contrasted with normal bone marrow indicators.

An analysis of a proposed diagnostic scheme for macrocytic anemia: sternal puncture, assessment of vitamin B12, folate, reticulocyte, and platelet levels.

Diagram of the indirect Coombs test (indirect antiglobulin test): detection of circulating incomplete antibodies to red blood cells and agglutination mechanism.

A table of medications causing immune hemolytic anemia and the importance of collecting a pharmacological history when the direct Coombs test is positive.

Urine sediment in paroxysmal nocturnal hemoglobinuria: microscopy of hemosiderin clumps in epithelial cells and a hyaline cast during hemolysis.

A flowchart for the differential diagnosis of anemia in pediatrics: evaluating reticulocytes, iron metabolism, myelogram, and erythrocyte morphology.

A hematology clinical case: evaluate complete blood count parameters in a 70-year-old patient with chronic lymphocytic leukemia and acute deterioration.

Erythrocyte morphology in sickle cell anemia: detection of drepanocytes, polychromatophilia, and normoblasts in a peripheral blood smear.

Morphological features of a binucleated megaloblast in bone marrow aspirate in pernicious anemia: chromatin structure and nuclear envelope.