Pituitary gonadal axis and child rate in males with classical 21-hydroxylase deficiency

Author:

Jääskeläinen Jarmo,Kiekara O.,Hippeläinen M.,Voutilainen R.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference23 articles.

1. New M.I. Steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia). Am. J. Med. 1995, 98: 2S–8S.

2. Jääskeläinen J., Levo A., Voutilainen R., Partanen J. Population-wide evaluation of disease manifestation in relation to molecular genotype in steroid 21-hydroxylase (CYP21) deficiency: good correlation in a well defined population. J. Clin. Endocrinol. Metab. 1997, 82: 3293–3297.

3. Holmes Walker D.J., Conway G.S., Honour J.W., Rumsby G., Jacobs H.S. Menstrual disturbance and hypersecretion of progesterone in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Clin. Endocrinol. (Oxf.) 1995, 43: 291–296.

4. Helleday J., Siwers B., Ritzen E.M., Carlstrom K. Subnormal androgen and elevated progesterone levels in women treated for congenital virilizing 21-hydroxylase deficiency. J. Clin. Endocrinol. Metab. 1993, 76: 933–936.

5. Mulaikal R.M., Migeon C.J., Rock J.A. Fertility rates in female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. N. Engl. J. Med. 1987, 316: 178–182.

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