Healthy Lifestyle Blog

What is Hereditary Spherocytosis (Minkowski-Chauffard Disease)? Hereditary spherocytosis (Minkowski-Chauffard disease) – hemolytic anemia due to a defect in the cell membrane of erythrocytes, the permeability of the membrane to sodium ions becomes excessive, and therefore

What is Hereditary Microspherocytosis? Hereditary microspherocytosis, also known as Minkowski – Chauffard disease, is a hereditarily determinable disease transmitted by an autosomal dominant type, characterized by a defect in the erythrocyte membrane proteins. As a

What is hereditary hemolytic anemia caused by the disturbance of the activity of erythrocyte enzymes? Reducing the activity of red blood cell enzymes usually entails a violation of ATP production in these red blood cells.

What is a Violation of Coagulation Hemostasis? This group includes genetically determined hypocoagulations, characterized by a deficiency, as well as molecular abnormalities of blood coagulation factors. Thus, 83-90% of all hereditary bleeding disorders are 2

What is Obstructive Jaundice? All types of obstructive jaundice, like other violations of the flow of bile into the intestine, lead to a drastic weakening or cessation of the absorption of vitamin K and the

What is Marching Hemoglobinuria? Marching hemoglobinuria is a rare form of mechanical hemolytic anemia with intravascular hemolysis due to injury of red blood cells in the capillaries of the feet. Hemoglobinuria, associated with prolonged walking,

What is Skin Lymphocytoma (Caesare’s Disease)? Lymphocytomas of the skin exist in several forms: lymphomatosis (lymphocytoma) of the skin such as Sesari disease, fungal mycosis, common B-cell lymphocytoma of the skin. Sesari disease can be

What is the Bug Origin of Hemoblastosis? Leukemia cells are a clone, that is, the offspring of a single mutated cell, and carry the characteristics of an originally mutated cell. Chromosomal analysis of acute leukemias

What is Factor XIII Deficiency? The disease was first described in 1960 by the scientist Duckert and co-authors, who identified 2 brothers with severe hemorrhagic diathesis, characterized by a hereditary deficiency of fibrin-stabilizing factor (factor

What is Factor VII Deficiency The disease was first described in 1951 by Alexander and co-authors. This is the only hemorrhagic diathesis with isolated prolongation of the prothrombin time (reduction of the prothrombin index) with