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SUN-360 Multi-Steroid Panels to Replace Dynamic Testing for the Diagnosis of Nonclassic 21-Hydroxylase Deficiency

Background: The diagnosis of nonclassic 21-hydroxylase deficiency (N21OHD) is considered in children with precocious pubarche, in the differential diagnosis of polycystic ovary syndrome, and in first-degree relatives of patients with 21OHD. Currently, the diagnosis of N21OHD requires cosyntropin (AC...

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Vydáno v:J Endocr Soc
Hlavní autoři: Turcu, Adina, El-Maouche, Diala, Nanba, Aya, Zhao, Lili, Merke, Deborah, Auchus, Richard
Médium: Artigo
Jazyk:Inglês
Vydáno: Endocrine Society 2019
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6553133/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-360
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