Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
J Steroid Biochem ; 35(6): 735-9, 1990 May.
Article in English | MEDLINE | ID: mdl-2362435

ABSTRACT

The diagnosis of non-classical 3 beta-hydroxysteroid dehydrogenase deficiency (NC-3BHSD) is made either on the basis of significantly elevated serum levels of basal and post-ACTH 5-ene-steroids or by the presence of elevated urinary 5-ene-steroid metabolites. There has been only one report to date describing a single patient where the diagnosis was based on both serum and urinary 5-ene-steroid levels. We, therefore, measured both serum 5-ene-steroid responses to ACTH 1-24 (by RIA) and urinary 5-ene-steroid metabolites (GC-MS) in 42 hirsute premenopausal women. While the serum 5-ene-steroid profile was consistent with NC-3BHSD in 5 women, only 2 of them had increased excretion of 5-ene-steroid metabolites. Elevated 5-ene-steroid excretion was also observed in several patients with normal serum 5-ene-steroids. Detection of NC-3BHSD by either elevated serum 5-ene-steroids or increased urinary excretion of their metabolites in isolation may not therefore be reliable.


Subject(s)
17-Ketosteroids/urine , 3-Hydroxysteroid Dehydrogenases/deficiency , Adrenal Hyperplasia, Congenital/diagnosis , Pregnenes/urine , 17-Ketosteroids/blood , Adolescent , Adrenal Hyperplasia, Congenital/blood , Adrenal Hyperplasia, Congenital/urine , Adult , Cosyntropin/pharmacology , Female , Humans , Male , Pregnenes/blood , Stimulation, Chemical
SELECTION OF CITATIONS
SEARCH DETAIL
...