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pubmed-article:6327799pubmed:abstractTextWe describe 5 adult women with severe hirsutism due to late onset 21-hydroxylase deficiency. Diagnosis was performed on the finding of high serum 17-hydroxyprogesterone (17OHP) levels with a marked hyperresponse to an ACTH test. The endocrine study showed in most patients a gonadotropin behavior similar to that observed in classical polycystic ovary (PCO) syndrome. Prolactin levels were slightly increased in basal conditions and presented an exaggerated response to TRH stimulation.lld:pubmed
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pubmed-article:6327799pubmed:articleTitleThe endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).lld:pubmed
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