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Screening for non-classic congenital adrenal hyperplasia in women: New insights using different immunoassays.
Nakhleh A, Saiegh L, Shehadeh N, Weintrob N, Sheikh-Ahmad M, Supino-Rosin L, Alboim S, Gendelman R, Zloczower M. Nakhleh A, et al. Front Endocrinol (Lausanne). 2023 Jan 10;13:1048663. doi: 10.3389/fendo.2022.1048663. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36704043 Free PMC article.
CONTEXT: The 250g-cosyntropin stimulation test (CST) is used to diagnose non-classic congenital adrenal hyperplasia (NCCAH). The current recommendation is to perform CST when follicular 17-hydroxyprogesterone (17OHP) is 6-30 nmol/L, a cutoff der …
CONTEXT: The 250g-cosyntropin stimulation test (CST) is used to diagnose non-classic congenital adrenal hyper …
The prevalence of non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Russian women with hyperandrogenism.
Grodnitskaya E, Kurtser M. Grodnitskaya E, et al. Hum Fertil (Camb). 2018 Dec;21(4):281-287. doi: 10.1080/14647273.2017.1344360. Epub 2017 Jul 3. Hum Fertil (Camb). 2018. PMID: 28669219
The aim of the study was to determine the prevalence of non-classic congenital adrenal hyperplasia (NCAH) due to 21-hydroxylase (21-OH) deficiency among hyperandrogenic women in a Russian population and to evaluate diagnostic value of basal seru …
The aim of the study was to determine the prevalence of non-classic congenital adrenal hyperplasia (NCAH) …
Body composition in children and adolescents with non-classic congenital adrenal hyperplasia and the risk for components of metabolic syndrome: An observational study.
Ben Simon A, Brener A, Segev-Becker A, Yackobovitch-Gavan M, Uretzky A, Schachter Davidov A, Alaev A, Oren A, Eyal O, Weintrob N, Lebenthal Y. Ben Simon A, et al. Front Endocrinol (Lausanne). 2022 Oct 20;13:1022752. doi: 10.3389/fendo.2022.1022752. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36353234 Free PMC article.
BACKGROUND: Treated or untreated non-classic congenital adrenal hyperplasia (NCCAH) diagnosed in childhood could pose an increased risk of obesity and metabolic derangements in adolescence and early adulthood. ...The linear regression models dep …
BACKGROUND: Treated or untreated non-classic congenital adrenal hyperplasia (NCCAH) diagnosed in childhoo …
Non-Classic Disorder of Adrenal Steroidogenesis and Clinical Dilemmas in 21-Hydroxylase Deficiency Combined with Backdoor Androgen Pathway. Mini-Review and Case Report.
Sumińska M, Bogusz-Górna K, Wegner D, Fichna M. Sumińska M, et al. Int J Mol Sci. 2020 Jun 29;21(13):4622. doi: 10.3390/ijms21134622. Int J Mol Sci. 2020. PMID: 32610579 Free PMC article. Review.
In 24 h urine collection, an increased excretion of 16alpha-OHDHEA-a dehydroepiandrosterone metabolite-and pregnanetriolone-a 17alpha-hydroxyprogesterone metabolite-were observed. The investigations that we undertook provided evidence that the girl suffered from non-classi …
In 24 h urine collection, an increased excretion of 16alpha-OHDHEA-a dehydroepiandrosterone metabolite-and pregnanetriolone-a 17alpha-hydrox …
Case Report: Anastrozole as a monotherapy for pre-pubertal children with non-classic congenital adrenal hyperplasia.
Liu SC, Suresh M, Jaber M, Mercado Munoz Y, Sarafoglou K. Liu SC, et al. Front Endocrinol (Lausanne). 2023 Mar 2;14:1101843. doi: 10.3389/fendo.2023.1101843. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36936152 Free PMC article.
Most children with non-classic congenital adrenal hyperplasia (NC-CAH) due to 21-hydroxylase deficiency are asymptomatic and do not require cortisol replacement therapy unless they develop symptoms of hyperandrogenemia. ...We present three pre-p …
Most children with non-classic congenital adrenal hyperplasia (NC-CAH) due to 21-hydroxylase deficiency a …
Genetic defects of the CYP21A2 gene in girls with premature adrenarche.
Skordis N, Shammas C, Phedonos AA, Kyriakou A, Toumba M, Neocleous V, Phylactou LA. Skordis N, et al. J Endocrinol Invest. 2015 May;38(5):535-9. doi: 10.1007/s40618-014-0223-1. Epub 2014 Dec 7. J Endocrinol Invest. 2015. PMID: 25481255
Direct DNA sequencing and MLPA analysis were performed to identify mutations in CYP21A2 gene. RESULTS: Twelve girls were diagnosed with non-classic congenital adrenal hyperplasia (NC-CAH) based on stimulated 17-hydroxyprogesterone (17-OHP) level …
Direct DNA sequencing and MLPA analysis were performed to identify mutations in CYP21A2 gene. RESULTS: Twelve girls were diagnosed with n …
Value of buserelin testing in the evaluation of hirsute women.
Ambrosi B, Re T, Passini E, Bochicchio D, Ferrario R. Ambrosi B, et al. J Endocrinol Invest. 1996 Apr;19(4):204-9. doi: 10.1007/BF03349868. J Endocrinol Invest. 1996. PMID: 8862498
Therefore, in 33 consecutive women with hirsutism serum LH, FSH, 17-OHP, dehydroepiandrosterone sulfate (DHEA-S), androstenedione (A), cortisol levels were evaluated in basal conditions and after the administration of buserelin (0.5 mg sc) and ACTH (tetracosactide 0.25 mg iv). Tw …
Therefore, in 33 consecutive women with hirsutism serum LH, FSH, 17-OHP, dehydroepiandrosterone sulfate (DHEA-S), androstenedione (A), corti …
The effect of simvastatin treatment on plasma steroid levels in females with non-classic congenital adrenal hyperplasia.
Krysiak R, Okopien B. Krysiak R, et al. Exp Clin Endocrinol Diabetes. 2013 Nov;121(10):643-6. doi: 10.1055/s-0033-1355383. Epub 2013 Sep 20. Exp Clin Endocrinol Diabetes. 2013. PMID: 24057511
Non-classic congenital adrenal hyperplasia (NC-CAH) is one of the most frequent genetic disorders and its presence often results in androgen excess. 4 females with coexisting symptomatic NC-CAH and isolated hypercholesterolemia and 11 sex- and w …
Non-classic congenital adrenal hyperplasia (NC-CAH) is one of the most frequent genetic disorders and its …
Combined oral contraceptive treatment of adolescent girls with polycystic ovary syndrome. Lipid profile.
Creatsas G, Koliopoulos C, Mastorakos G. Creatsas G, et al. Ann N Y Acad Sci. 2000;900:245-52. doi: 10.1111/j.1749-6632.2000.tb06236.x. Ann N Y Acad Sci. 2000. PMID: 10818412 Clinical Trial.
They were all hyperandrogenic and euthyroid and had normal prolactin plasma levels. Non-classic congenital adrenal hyperplasia was ruled out by the ACTH stimulation test. ...Our data show that after 12 months of treatment with the D or CA COC, t …
They were all hyperandrogenic and euthyroid and had normal prolactin plasma levels. Non-classic congenital adrenal …
A case of recurrent labial adhesions in a 15-month-old child with asymptomatic non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Janus D, Wojcik M, Malunowicz E, Starzyk JB. Janus D, et al. J Pediatr Endocrinol Metab. 2012;25(9-10):1017-21. doi: 10.1515/jpem-2012-0190. J Pediatr Endocrinol Metab. 2012. PMID: 23426836
Urinary steroid profile and molecular analysis confirmed the diagnosis of non-classic congenital adrenal hyperplasia (NCCAH) due to 21-hydroxylase deficiency. ...However, it seems that in cases of recurrent labial adhesion/synechia that require …
Urinary steroid profile and molecular analysis confirmed the diagnosis of non-classic congenital adrenal hype …