Congenital adrenal hyperplasia due to combined 21- and 11 ß-hydroxylase deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://link.springer.com/content/pdf/10.1007/BF03350043.pdf
Reference32 articles.
1. White C.W., New M.I., Dupont B. Congenital adrenal hyperplasia. N. Engl. J. Med. 316: 1519 and 1580, 1987.
2. Fukushima D.K., Nishina T., Wu R.H.K., Hellman L., Finkelstein J.W. Rapid assay of plasma 21-deoxycortisol and 11-deoxycortisol in congenital adrenal hyperplasia. Clin. Endocrinol. (Oxf.) 10: 367, 1979.
3. Gandy H.M., Keutmann E.H., Izzo A.J. Characterization of urinary steroids in adrenal hyperplasia: Isolation of metabolites of Cortisol, compound S, and deoxycorticosterone from a normotensive patient with adrenogenital syndrome. J.Clin. Invest. 39: 364, 1960.
4. Hurwitz A., Brautbar C., Milwidsky A., Vecesi P., Milewicz A., Navot D., Rosier A. Combined 21- and 11 ß-hydroxylase deficiency in familial congenital adrenal hyperplasia. J. Clin. Endocrinol. Metab. 60: 631, 1985.
5. Finkelstein M., Litvin Y., Mizrachi Y., Neiman G., Rosier A. Apparent double defect in CM- and C21-steroid hydroxylation in congenital adrenal hyperplasia. J. Steroid Biochem. 19: 675, 1983.
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