Healthy Blog

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

What is Hyperprolactinemic Hypogonadism? Hyperprolactinemic hypogonadism was isolated in a separate form of central hypogonadism only in recent years by the development of laboratory radioimmunological diagnostics in endocrinology. Causes of Hypogonadism of Hyperprolactinemic Syndrome of

What is Hypogonadism? Hypogonadism is a collective concept that includes all conditions accompanied by hypofunction of the testicles. Causes of Hypogonadism Hypogonadism includes conditions caused by the pathology of the testicles proper or the function