2023-09-182023-09-182013-09-27Eren, E. vd. (2013). "Etiological evaluation of adolescents with primary amenorrhea". Indian journal of pediatrics, 81(9), 861-865.0019-54560973-7693https://doi.org/10.1007/s12098-013-1266-6https://link.springer.com/article/10.1007/s12098-013-1266-6http://hdl.handle.net/11452/33871Objectives To determine causes of amenorrhea in adolescents with primary amenorrhea and to emphasize general approach to primary amenorrhea. Methods Thirty-nine patients, evaluated between January 2007 and May 2011, were divided into normogonadotropic hypogonadism, hypergonadotropic hypogonadism and hypogonadotropic hypogonadism groups. Means of age, height, weight, body mass index and standard deviation scores, gonadotropin levels, and accompanying diseases were evaluated. Results Mean values of age, height, height standard deviation score, weight and, weight standard deviation score were 15.54 +/- 1.52 y. 152.0 +/- 1.1 cm, -1.37 +/- 1.3, 48.2 +/- 14.3 kg, 0.96 +/- 1.75, respectively. There were no statistical significances in the auxological parameters. Patients were distributed as 18 cases (46.1 %) with normogonadotropic hypogonadism, 12 cases (30.8 %) with hypergonadotropic hypogonadism, 9 cases (23.1 %) with hypogonadotropic hypogonadism. In the group of normogonadotropic hypogonadism, there were 6 patients with chronic diseases, 5 patients with insulin resistance, 4 patients with prolactinomas, 3 patients with mullerian agenesis. Of the hypergonadotropic hypogonadic patients, 3 were idiopathic primary ovarian failure, 3 were 46, XY disorders of sex development, 2 were Turner syndrome, 2 were ovarian insufficiency due to drug, one was 17 alpha-hydroxylase deficiency and one was autoimmune oophoritis. The group of hypogonadotropic hypogonadism included 5 patients with normosmic hypogonadism, 2 patients with constitutional delay of growth and puberty, 1 patient with panhypopituitarism and 1 patient with anosmic hypogonadism. Conclusions Chronic diseases, prolactinoma, and insulin resistance may lead to hypogonadism without altering gonadotropin levels. Turner syndrome, primary ovarian failure, and autoimmune oophoritis should be investigated in cases with hypergonadotropic hypogonadism. 46, XY disorders of sex development also should be elucidated. Constitutional delay of growth and puberty should be distinguished from isolated hypogonadotropic hypogonadism.eninfo:eu-repo/semantics/closedAccessAmenorrheaProlactinomaAdolescentHypogonadismInsulin resistanceOvarian syndromeMenstruationPediatricsAdolescentAmenorrheaFemaleHumansHypogonadismArticle0003416335000042-s2.0-8502824730986186581924178309PediatricsPrimary Ovarian Insufficiency; Gene; Ovarian ReserveAdolescentAmenorrheaComplicationFemaleHumanHypogonadism