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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1984-7-25
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pubmed:abstractText |
We 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.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0391-4097
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
89-92
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6327799-17-alpha-Hydroxyprogesterone,
pubmed-meshheading:6327799-Adolescent,
pubmed-meshheading:6327799-Adrenal Hyperplasia, Congenital,
pubmed-meshheading:6327799-Adrenocorticotropic Hormone,
pubmed-meshheading:6327799-Adult,
pubmed-meshheading:6327799-Female,
pubmed-meshheading:6327799-Follicle Stimulating Hormone,
pubmed-meshheading:6327799-Gonadal Steroid Hormones,
pubmed-meshheading:6327799-Hirsutism,
pubmed-meshheading:6327799-Humans,
pubmed-meshheading:6327799-Hydroxyprogesterones,
pubmed-meshheading:6327799-Luteinizing Hormone,
pubmed-meshheading:6327799-Prolactin,
pubmed-meshheading:6327799-Steroid 21-Hydroxylase,
pubmed-meshheading:6327799-Steroid Hydroxylases
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pubmed:year |
1984
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pubmed:articleTitle |
The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).
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pubmed:publicationType |
Journal Article
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