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Cognitive Impairement in Central Hypogonadis in Male Associated with Pitutary Tumor
Male hypogonadism has a multifactorial etiology that icludes genetic conditions, anatomic abnormalities, infection, tumor, and injury. Tumors of the pituitary cause hypogonalism by by either mass effect or distruction of gonadotropes or by hormonal production, which inhibits the GnRH pulse generator. The nanifests of hypogonadism are testisterone deficiency, infertility, or both. Signs and symptoms of this condition depend on whether it occured before or after the onset of puberty. Androgen therapy in needed in all HH patients. Testosterone is the primary treatment to indure and maintain secondary sexual characteristics and sexual function in men with hypogonadism.
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