Category: Medicine

What is Gangliosidosis GM2 Type II (Sandhoff Disease)? Gangliosidosis GM2 type II (Sandhoff’s Disease) is a hereditary disease from the group of gangliosidosis. Causes of Gangliosidosis GM2 Type II (Sandhoff Disease) Sandhoff’s disease (GM2-gangliosidosis, type

What is Gangliosidosis GM1 Type I? GM1-gangliosidosis type I (generalized familial gangliosidosis, neurovisceral lipidosis, b-galactosidase deficiency) is characterized by an autosomal recessively inherited deficiency of the enzyme GM1-b-galactosadase. The activity of this enzyme in the

What is Molybdenum Deficiency? Molybdenum is an element of the VI group of the periodic system; at. n – 42, at. m. – 96. The name comes from the Greek. molybdos (lead). Highlighted by P.

What is Iron Deficiency? Anemia is an iron deficiency in the body. Anemia, or anemia, is a pathological condition characterized by a decrease in hemoglobin concentration and, in the vast majority of cases, the number

What is Lactacidemic Coma? Lactacidemic coma is associated with the highest mortality rate – mortality can reach 80%. The state of lactic acidosis can be ascertained when the level of lactic acid in the blood

What is Kwashiorkor? Kwashiorkor is a type of severe dystrophy. The disease usually occurs in children 1-4 years old, although it happens that it occurs at an older age (for example, in adults or in

What is Dwarfism (Stunting)? Dwarfism (short stature, pituitary dwarfism) is a disease characterized by stunted growth and physical development. Dwarf consider growth of an adult man below 130 cm, adult women – below 120 cm.

What is Magnesium Deficiency? In recent years, close attention of researchers in various fields of clinical medicine has been attracted to the problem of magnesium deficiency and its role in the formation of various pathological

What is Type I Glycogenosis (Girke’s Disease)? Type I glycogenosis is a disease described by Girke in 1929, but Cory only discovered the enzyme defect in 1952. Type I glycogenosis occurs in 1 out of

What is Gaucher Disease (Glucocerebroside Lipidosis, Glucocerebrosidosis)? Gaucher disease (glucocerebrosid lipidosis, glucocerebrosidosis) is one of the most frequent inherited disorders of glycolipid metabolism. It is believed that Gaucher disease is based on allelic mutations of