Author: treatment-diabetes

What is Hereditary Pyropoikilocytosis? This is a rare hereditary hemolytic anemia associated with impaired protein structure of the erythrocyte membrane; it is accompanied by severe intracellular destruction of red blood cells and low resistance of

What is the Inherited Lecithin-Cholesterol-Acyltransferase Activity Deficit? The hereditary deficiency of lecithin-cholesterol-acyltransferase activity is a recessively inherited defect, which was first described in 1967. In addition to hemolytic anemia, patients have a violation of cornea

What is Hereditary Coproporphyria? The extremely rare form of porphyria was first described in 1955. According to clinical signs, the disease resembles acute intermittent porphyria. Causes of Hereditary Coproporphyria The disease is genetically determined, is

What is Myeloma? Myeloma (from ancient Greek. – bone marrow and ending in the names of tumors), Rustitsky-Kalera disease, multiple myeloma, generalized plasma cytoma – a disease of the blood system, related to paraproteinemic leukemia.

What is Mastocytosis (Mast Cell Leukemia)? Mastocytosis (mast cell leukemia) is a systemic disease, the morphological substrate of which is massive infiltration of the skin, various organs and tissues with fat cells (mast cells, labrocytes,

What is a Lymphocytoma of the Lymph Node? Lymphocytoma of the lymph node is often diagnosed as chronic lymphocytic leukemia or as lymphosarcoma. Like other lymphocyte forms, this benign non-leukemic form of lymphatic proliferation lasts

What is Leukopenia and Agranulocytosis? The proportion of leukopenic conditions among other diseases of the blood system is quite large. Statistics show an increase in the number of patients with severe leukopenia in recent years.

What are the Patterns of Tumor Progression? Hemoblastosis has two stages: monoclonal (benign) and polyclonal – the occurrence of subclones (malignant). However, the change of stages is carried out with an unequal frequency in different

What is Deficiency Factor XI? The disease was first described in 1953 by Rosenthal scientists and co-authors. Since 1962, according to the International Nomenclature, this factor is denoted by the number XI. Inheritance The disease

What is Factor I Deficiency? Congenital and hereditary forms of fibrinogen deficiency are described as early as 1920. Family afibrinogenemia (absence of fibrinogen in the blood plasma) is a rare disease that is inherited in