Healthy Blog

What is Diffuse (Endemic) Goiter? Endemic goiter is an enlargement of the thyroid gland that develops as a result of iodine deficiency in people living in certain geographical areas with iodine deficiency in the environment

What is Protein-energy Deficiency? With insufficient intake of protein and energy, lean body mass and the amount of adipose tissue are reduced, and one of these changes may be more pronounced. Protein deficiency is a

What is Type X Glycogenosis? Type X glycogenosis is a hereditary disease that is caused by a lack of enzymes involved in glycogen metabolism; characterized by a violation of the structure of glycogen, insufficient or

What is Type VII Glycogenosis (Tarui Disease, Myophosphofructokinase Deficiency)? Type VII glycogenosis (Tarui disease, myophosphofructokinase deficiency) is a hereditary disease, which is caused by a lack of enzymes involved in the metabolism of glycogen; characterized

What is Type VI Glycogenosis (Herce’s Disease, Hepatophosphorylase Insufficiency)? Type VI glycogenosis (Hers disease, hepatophosphorylase insufficiency) – glycogenosis caused by liver phosphorylase deficiency. Pathogenesis during Type VI Glycogenosis (Herce’s Disease, Hepatophosphorylase Insufficiency) Liver phosphorylase catalyzes

What is Type II Glycogenosis (Pompe Disease)? Pompe disease is type II glycogenosis, a rare genetic metabolic disorder, caused by the congenital absence of the enzyme lysosomal alpha-glucosidase, which is necessary to destroy glycogen, a

What is Type 0 Glycogenosis (aglycogenosis)? Aglycogenosis is a hereditary disease caused by the absence of an enzyme responsible for the synthesis of glycogen, namely uridine diphosphate glucose glycogen transferase or glycogen synthetase. This disease

What is Hypopituitarism? Hypopituitarism syndrome is a disease characterized by a decrease and loss of function of the anterior pituitary or adenohypophysis. The pituitary gland or the pituitary gland consists of two lobes of the

What is Hypokalemia? Hypokalemia is a condition in which the concentration of potassium in the plasma is below 3.5 mmol / L. Hypokalemia causes severe complications (for example, life-threatening ventricular arrhythmias). Clinical signs of hypokalemia

What is Primary Congenital Hypogonadism (Anorchism)? Congenital absence of testicles (born anorchism, anorchia, intrauterine anorchism) in pheno- and genotypic boys is a rare pathology: 1 in 20 thousand children. The etiology of anorchism syndrome is