Partial 17, 20-desmolase and 17α-hydroxylase deficiencies in a 16-year-old boy-Reference-Cited by-同舟云学术

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Partial 17, 20-desmolase and 17α-hydroxylase deficiencies in a 16-year-old boy

Published:1988-07 Issue:7 Volume:11 Page:527-533
ISSN:0391-4097
Container-title:Journal of Endocrinological Investigation
language:en
Short-container-title:J Endocrinol Invest

Author:

Bosson D.,Wolter R.,Toppet M.,Franckson J. R. M.,de Peretti E.,Forest M. G.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/content/pdf/10.1007/BF03350177.pdf

Reference45 articles.

1. Zachmann M., Vollmin J.A., Hamilton W., Prader A. Steroid 17, 20-desmolase deficiency: a new case of male pseudohermaphroditism. Clin. Endocrinol. (Oxf) 1: 369, 1972.

2. Goebelsmann U., Zachmann M., Davajan V., Israël R., Mestman J.H., Mishell D.R. Male pseudohermaphroditism consistent with 17, 20-desmolase deficiency. Gynecol. Invest. 7: 138, 1976.

3. Forest M.G., Lecornu M., de Peretti E. Familial male pseudohermaphroditism due to 17, 20-desmolase deficiency. I. In vivo endocrine studies. J. Clin. Endocrinol. Metab. 50: 826, 1980.

4. David M., Forest M.G., Zachmann M., de Peretti E. 17, 20-desmolase deficiency in two unrelated prepubertal and adolescent boys previously diagnosed as simple hypospadias. Pediatr. Res. 15: 83, 1981, (abstract).

5. Campo S., Moteagudo C., Nicolau G., Pellizzari E., Belgorosky A., Stivel M., Rivarola M. Testicular function in prepubertal male pseudohermaphroditism. Clin. Endocrinol. (Oxf.) 14: 11, 1981.

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