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Hyperandrogenism and Adrenocortical Tumors
2019Androgen-secreting tumors are a rare cause of hyperandrogenism of adrenal origin. Although these tumors are identified in less than 2% of patients, the prevalence of adrenocortical carcinomas is relevant (2/3 of the cases). Those tumors are associated with simultaneous elevation of several androgens, mainly androstenedione, DHEAS, and testosterone, in ...
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Current Opinion in Obstetrics and Gynecology, 1992
Mutations in the genes for the insulin receptor, 21-hydroxylase, 11 beta-hydroxylase, and 3 beta-hydroxysteroid dehydrogenase isomerase enzymes are associated with hyperandrogenism. These genetic causes of hyperandrogenism account for less than 10% of all cases.
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Mutations in the genes for the insulin receptor, 21-hydroxylase, 11 beta-hydroxylase, and 3 beta-hydroxysteroid dehydrogenase isomerase enzymes are associated with hyperandrogenism. These genetic causes of hyperandrogenism account for less than 10% of all cases.
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Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
Journal of Clinical Endocrinology and Metabolism, 2023Angelica Lindén Hirschberg
exaly
2019
The differential diagnosis of the hyperandrogenic patient includes idiopathic hirsutism, polycystic ovary syndrome (PCOS), the hyperandrogenic insulin-resistant acanthosis nigricans (HAIRAN) syndrome, 21-hydroxylase-deficient non-classic congenital adrenal hyperplasia or classic congenital adrenal hyperplasia, and androgen-secreting neoplasm.
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The differential diagnosis of the hyperandrogenic patient includes idiopathic hirsutism, polycystic ovary syndrome (PCOS), the hyperandrogenic insulin-resistant acanthosis nigricans (HAIRAN) syndrome, 21-hydroxylase-deficient non-classic congenital adrenal hyperplasia or classic congenital adrenal hyperplasia, and androgen-secreting neoplasm.
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Practical Approach to Hyperandrogenism in Women
Medical Clinics of North America, 2021Corrine K. Welt
exaly

