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Year Number of Results
2016 1
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2019 1
2020 1
2022 2
2023 2
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Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women.
Carmina E, Dewailly D, Escobar-Morreale HF, Kelestimur F, Moran C, Oberfield S, Witchel SF, Azziz R. Carmina E, et al. Hum Reprod Update. 2017 Sep 1;23(5):580-599. doi: 10.1093/humupd/dmx014. Hum Reprod Update. 2017. PMID: 28582566 Review.
BACKGROUND: Non-classic congenital hyperplasia (NCAH) due to 21-hydroxylase deficiency is a common autosomal recessive disorder characterized by androgen excess. ...Definitive diagnosis requires a 17-OHP concentration 10 ng/ml (30 nmol/l), either basal …
BACKGROUND: Non-classic congenital hyperplasia (NCAH) due to 21-hydroxylase deficiency is a common autosomal recessive …
Ethnic and National Differences in Congenital Adrenal Hyperplasia Incidence: A Systematic Review and Meta-Analysis.
Navarro-Zambrana AN, Sheets LR. Navarro-Zambrana AN, et al. Horm Res Paediatr. 2023;96(3):249-258. doi: 10.1159/000526401. Epub 2022 Aug 16. Horm Res Paediatr. 2023. PMID: 35973409 Free article.
Cultural practices in some places regarding consanguineous unions or geographic isolation may directly affect the incidence. Newborn screening for CAH may be unavailable in many developing countries, thereby affecting the actual CAH incidence. Therefore, healthcare workers …
Cultural practices in some places regarding consanguineous unions or geographic isolation may directly affect the incidence. Newborn scre …
Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review.
Papadakis G, Kandaraki EA, Tseniklidi E, Papalou O, Diamanti-Kandarakis E. Papadakis G, et al. Front Endocrinol (Lausanne). 2019 Jun 19;10:388. doi: 10.3389/fendo.2019.00388. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31275245 Free PMC article.
Search terms were "polycystic ovary syndrome," "PCOS," "non-classical adrenal hyperplasia," "NC-CAH," "21-hydroxylase deficiency." From an initial 16,255 titles, the evaluations led to the final inclusion of 97 papers. ...Conclusions: The screening too …
Search terms were "polycystic ovary syndrome," "PCOS," "non-classical adrenal hyperplasia," "NC-CAH," "21-hydroxylase defic …
Mutation distributions among patients with congenital adrenal hyperplasia from five regions of Brazil: a systematic review.
Hosomi SS, Salles IC, Bachega TASS. Hosomi SS, et al. Arch Endocrinol Metab. 2023 Mar 30;67(3):427-441. doi: 10.20945/2359-3997000000593. Arch Endocrinol Metab. 2023. PMID: 37011374 Free PMC article. Review.
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency is an autosomal recessive disorder caused by CYP21A2 gene mutations, and its molecular diagnosis is widely used in clinical practice to confirm the hormo …
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency is an autosomal rece …
CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY PRESENTING AS ADRENAL INCIDENTALOMA: A SYSTEMATIC REVIEW AND META-ANALYSIS.
Falhammar H, Torpy DJ. Falhammar H, et al. Endocr Pract. 2016 Jun;22(6):736-52. doi: 10.4158/EP151085.RA. Epub 2016 Feb 26. Endocr Pract. 2016. PMID: 26919651
RESULTS: Thirty-six publications were included. Of AI patients biochemically screened for CAH, 58/990 (5.9%) were diagnosed with CAH. Genetic screening of all AIs revealed only 2/252 (0.8%) with clear CAH. ...Screening with 17-hydroxyprogesterone levels appea …
RESULTS: Thirty-six publications were included. Of AI patients biochemically screened for CAH, 58/990 (5.9%) were diagnosed with CAH. …
Glucocorticoid replacement regimens for treating congenital adrenal hyperplasia.
Ng SM, Stepien KM, Krishan A. Ng SM, et al. Cochrane Database Syst Rev. 2020 Mar 19;3(3):CD012517. doi: 10.1002/14651858.CD012517.pub2. Cochrane Database Syst Rev. 2020. PMID: 32190901 Free PMC article.
SELECTION CRITERIA: Randomised controlled trials (RCTs) or quasi-RCTs comparing different glucocorticoid replacement regimens for treating CAH due to 21-hydroxylase deficiency in children and adults. DATA COLLECTION AND ANALYSIS: The authors independently ext …
SELECTION CRITERIA: Randomised controlled trials (RCTs) or quasi-RCTs comparing different glucocorticoid replacement regimens for treating C …