17-α-hydroxylase deficiency in three siblings: short- and long-term studies

Author:

Scaroni C.,Biason A.,Carpenè G.,Opocher G.,Mantero F.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference33 articles.

1. Biglieri E.G., Herron H.A., Brust N. 17-α-hydroxylation in man. J. Clin. Invest. 45: 1946, 1966.

2. Mills I.H., Wilson R.J., Tait A.D., Cooper H.R. Steroid metabolic studies in a patient with 17-α-hydroxylation deficiency. J.Endocrinol. 38: 19, 1967.

3. Goldsmith O., Solomon D.H., Horton R. Hypogonadism and mineralocorticoid excess. The 17-hydroxylase deficiency syndrome. N. Engl. J. Med. 277: 673, 1967.

4. Rovner D.R., Conn J.W., Cohen E.L., Berlinger F.G., Kern D.C. Biglieri’s syndrome: unexplained by 17-α-hydroxylase defect alone. J. Lab. Clin. Med. 72: 1009, 1968.

5. Mallin S.R. Congenital adrenal hyperplasia secondary to 17-hydroxylase deficiency. Ann. Intern. Med. 49: 1930, 1969.

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