Month: March 2019

Among the tumors of the hypothalamic region, in addition to the craniopharyngioma, there are gliomas, hemangiomas, dysgerminomas, hamartomas, ganglion neurinomas, ependymomas, medulloblastomas, lipomas, neuroblastomas, lymphomas, plasmacytomas, colloid and dermoid cysts, sarcomas. Depending on the location

Acromegaly and gigantism are neuroendocrine syndromes resulting from excessive production or increased biological activity of growth hormone. These two diseases should be considered as age-related variations of the same pathological process, the specific clinical manifestations

Hypothalamic-hypophysial insufficiency (panhypopituitalism) is a clinical syndrome that develops as a result of destruction of the adenohypophysis, followed by a persistent decrease in the production of tropic hormones and impaired activity of the peripheral endocrine

Growth Failure Growth deficiency (growth hormone deficiency) occurs with a large number of diseases and syndromes. According to etiology, congenital and acquired as well as organic and idiopathic growth hormone deficiency are distinguished. In the

Definition Juvenile gynecomastia is any visible or palpable one- or two-sided increase in the mammary gland in boys and in young males. Synonym: pubertal gynecomastia, transient gynecomastia. Spread. 75% of adolescent boys have transient gynecomastia.

Gynecomastia must be distinguished from cancer, adenofibromas, adenomas, cystic mastopathy. The mastitis of young men is closely related to the early stage of gynecomastia, which in most cases takes place upon the onset of puberty.

Hyperinsulinism is a pathological condition of the body, caused by an absolute or relative excess of insulin, causing a strong decrease in blood sugar, resulting in glucose deficiency and oxygen starvation of the brain, leading