Pregnancy in a woman with congenital adrenal hyperplasia with 11-beta-hydroxylase deficiency: A case report

1. Merke, DP, Bornstein, SR. Congenital adrenal hyperplasia. Lancet 2005; 365: 2125–2136.
Google Scholar | Crossref | Medline | ISI2. Falhammar, H, Thoren, M. Clinical outcomes in the management of congenital adrenal hyperplasia. Endocrine 2012; 41: 355–373.
Google Scholar | Crossref | Medline3. Menabo, S, Polat, S, Baldazzi, L, et al. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations. Eur J Hum Genet 2014; 22: 610–616.
Google Scholar | Crossref | Medline4. De Crecchio, L . Sopra un caso di apparenze virili in una donna. Il Morgagni 1865; 7: 151–189.
Google Scholar5. Wilkins, L, Lewis, RA, Kelin, R, et al. Treatment of congenital hyperplasia with cortisone. J Clin Endocrinol Metab 1951; 11: 1–25.
Google Scholar | Crossref | Medline | ISI6. Bongiovanni, AM, Eberlein, WR. Plasma and urinary corticosteroids in the hypertensive form of congenital adrenal hyperplasia. J BiolChem 1956; 223: 85–94.
Google Scholar | Medline7. Krone, N, Arlt, W. Genetics of congenital adrenal hyperplasia. Best Pract Res Clin Endocrinol Metab 2009; 23: 181–192.
Google Scholar | Crossref | Medline | ISI8. White, PC . Steroid 11-beta-hydroxylase deficiency and related disorders. Endocrinol MetabClin North Am 2001; 30: 61–79.
Google Scholar | Crossref | Medline9. Peter, M . Congenital adrenal hyperplasia: 11-beta-hydroxylase deficiency. Semin Repord Med 2002; 20: 249–254.
Google Scholar | Crossref | Medline10. Simm, PJ, Zacharin. Successful pregnancy in a patient with severe 11-beta-hydroxylase deficiency and novel mutations in CYP11B1 gene. Horm Res 2007; 68: 294–297.
Google Scholar | Medline11. Toaff, ME , et al. Congenital adrenal hyperplasia caused by 11-beta-hydroxylase deficiency with onset of symptoms after one spontaneous pregnancy. Am J Obstet Gynecol 1975; 121: 202–204.
Google Scholar | Crossref | Medline12. Razzaghy-Azar, M , et al. Gender identity in patients with congenital adrenal hyperplasia. Int J Endocrinol Metab 2017; 15(3): e12537. doi:10.5812/ijem.12537.
Google Scholar13. aae, E , et al. Sexual orientation in individuals with congenital adrenal hyperplasia: a systematic review. Front Behav Neurosci 2020; 14: 38.
Google Scholar | Crossref | Medline14. Hagenfeldt, K , et al. Fertility and pregnancy outcome in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Reprod 2008; 23: 1607–1613.
Google Scholar | Crossref | Medline | ISI15. Lo, JC , et al. Pregnancy outcomes in women with congenital virilising adrenal hyperplasia. Endocrinol Metab Clin North Am 2001; 30: 207–229.
Google Scholar | Crossref | Medline | ISI16. Speiser, PW , et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an endocrine society clinical practise guideline. J Clin Endocrinol Metab 2010; 95: 4133–4160.
Google Scholar | Crossref | Medline | ISI17. Simpson, JL , et al. Prenatal genetic testing and treatment for congenital adrenal hyperplasia. Fertil Steril 2019; 111: 21–23.
Google Scholar | Crossref | Medline

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