Adrenal insufficiency in a man with non-classical 21-hydroxylase deficiency: Consequence or coincidence?-Reference-Cited by-同舟云学术

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Adrenal insufficiency in a man with non-classical 21-hydroxylase deficiency: Consequence or coincidence?

Published:1994-09 Issue:8 Volume:17 Page:665-670
ISSN:0391-4097
Container-title:Journal of Endocrinological Investigation
language:en
Short-container-title:J Endocrinol Invest

Author:

Glass Allan R.,Jackson S. G.,Perlstein R. S.,Wray H. Linton

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/content/pdf/10.1007/BF03349683.pdf

Reference17 articles.

1. Kohn B., Levine L.S., Pollack M.S., Pang S., Lorenzen F., Levy D., Lerner A.J., Rondanini G.F., Dupont B., New M.I. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia. J. Clin. Endocrinol. Metab. 55: 817, 1982.

2. Chrousos G.P., Loriaux D.L., Mann D.L., Cutler G.B. Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease: an allelic variant of congenital virilizing adrenal hyperplasia with a milder enzymatic defect. Ann. Intern. Med. 96: 143, 1982.

3. Lee P.A., Rosenwaks Z., Urban M.D., Migeon C.J., Bias W.D. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J. Clin. Endocrinol. Metab. 55:866, 1982.

4. Brodie B.L., Wentz A.C. Late onset congenital adrenal hyperplasia: a gynecologist’s perspective. Fertil. Steril. 48: 175, 1987.

5. Wu D.A., Chung B.C. Mutations in P450c21 (steroid 21-hydroxylase) at cys 428, val 281, and ser 268 result in complete, partial, or no loss of enzymatic activity, respectively. J.Clin. Invest. 88: 519, 1991.

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Coexistence of 21 Hydroxylase Deficiency and Autoimmune Adrenalitis: A Case Report;Journal of Diabetes and Endocrine Practice;2024-09-02

2. Genotype-Specific Cortisol Reserve in a Cohort of Subjects With Nonclassic Congenital Adrenal Hyperplasia (NCCAH);The Journal of Clinical Endocrinology & Metabolism;2023-09-16

3. Cortisol response to adrenocorticotropin testing in non-classical congenital adrenal hyperplasia (NCCAH);Journal of Pediatric Endocrinology and Metabolism;2016-01-01

4. Inadequate Cortisol Response to the Tetracosactide (Synacthen�) Test in Non-Classic Congenital Adrenal Hyperplasia: An Exception to the Rule?;Hormone Research in Paediatrics;2015-02-07

5. Development of Graves' Hyperthyroidism Caused an Adrenal Crisis in a Patient with Previously Unrecognized Non-classical 21-hydroxylase Deficiency;Internal Medicine;2010

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