Secondary hypogonadism Secondary hypogonadism is a syndrome caused by a decrease in the production of gonadotropic hormones of the anterior pituitary gland, resulting in a sharp decrease in estrogen secretion by the ovaries, and characterized

Primary hypogonadism Primary hypogonadism is a syndrome caused by the direct effect of the pathological process on ovarian function, as a result of which a sharp decrease in estrogen secretion occurs. Etiology. Primary ovarian failure

Pathological menopause Climax – a normal physiological state of the body, the transition from reproductive period to menopause. It is caused by the age-related involutional rearrangement in the higher parts of the central nervous system,

Early puberty Stein-Leventhal syndrome is characterized by menstrual disorders, infertility, bilateral ovarian enlargement, hirsutism in the female phenotype. The syndrome occurs in 1.45–2.8% of all gynecological diseases; it occurs in women more often at the

Hormonally active ovarian tumors Ovarian granulocellular tumor is a tumor arising from the granulosa cells of the follicles or from embryonic remnants of granulosa cells that are not associated with the follicles. Tecoma is a

Arrhenoblastoma Arrhenoblastoma is a tumor emanating from the male elements of the female gonad. It is the most common virilizing ovarian tumor. Arrhenoblastoma develops at any age, often in childbearing. Etiology. The cause of the

Male Genital Gland Disease The testicles are a paired glandular organ located in the moson ke. In men, the length of the testicle is 3-5 cm, width – 2-3 cm, and weight – 15-30 g.

Primary hypogonadism Primary hypogonadism is a syndrome caused by the direct effect of the pathological process on the testicular parenchyma. Etiology. The causes of primary hypogonadism can be congenital and acquired. Congenital causes of testicular

Secondary hypogonadism Secondary hypogonadism – a syndrome that occurs mainly due to hypothalamic-pituitary insufficiency, leading to a decrease in the production of gonadotropic hormones, followed by a decrease in the secretion of androgens. Etiology. The

Cryptorchidism True cryptorchidism – congenital dystopia of the testicles, their location outside the scrotum. In true cryptorchidism, the testicle is permanently located in the inguinal canal or abdominal cavity. When false cryptorchidism in the inguinal