Late consequences of classic congenital adrenal hyperplasia and its long-term poor control in men (case report and literature review)

Author:

Shifman Boris M.1ORCID,Dzeranova Larisa K.1ORCID,Pigarova Ekaterina A.1ORCID,Tiulpakov Anatoly N.2ORCID,Fedorova Natalia S.2ORCID

Affiliation:

1. Endocrinology Research Centre

2. Endocrynology Research Centre

Publisher

Endocrinology Research Centre

Subject

Public Health, Environmental and Occupational Health,Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference93 articles.

1. Mel'nichenko G.A., Troshina E.A., Molashenko N.V., i dr. Klinicheskie rekomendatsii Rossiiskoi Assotsiatsii endokrinologov po diagnostike i lechebno-profilakticheskim meropriyatiyam pri vrozhdennoi disfunktsii kory nadpochechnikov u patsientov vo vzroslom vozraste. // Consilium Medicum. – 2016. – T.18. – № 4. – S. 8–19. [Mel’nichenko GA, Troshina EA, Molashenko NV, et al. Russian Association of Endocrinologists clinical practice guidelinesfor diagnosis, treatment and preventive measures in congenital adrenal hyperplasia due to 21-hydroxylase deficiency patients in adulthood. Consilium Medicum. 2016;18(4):8-19. (In Russ).]

2. Speiser PW, Arlt W, Auchus RJ, et al. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline. J Clin Endocrinol Metab. 2018;103(11):4043-4088. DOI:10.1210/jc.2018-01865

3. Arlt W, Willis DS, Wild SH, et al. Health Status of Adults with Congenital Adrenal Hyperplasia: A Cohort Study of 203 Patients. J Clin Endocrinol Metab. 2010;95(11):5110-5121. DOI:10.1210/jc.2010-0917

4. Witchel SF. Congenital Adrenal Hyperplasia. J Pediatr Adolesc Gynecol. 2017;30(5):520-534. DOI:10.1016/j.jpag.2017.04.001

5. Tusie-Luna MT, Traktman P, White PC. Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus. J Biol Chem. 1990;265(34):20916-20922.

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