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A new variant of 17 alpha-hydroxylase deficiency with hyperaldosteronism in two Japanese sisters.

作者信息

Monno S, Takasu N

机构信息

Department of Internal Medicine, School of Medicine, Shinshu University, Matsumoto, Japan.

出版信息

Endocrinol Jpn. 1989 Apr;36(2):315-23. doi: 10.1507/endocrj1954.36.315.

Abstract

We present a report on two sisters who have 17 alpha-hydroxylase deficiency with hyperaldosteronism. They have hypertension and hypergonadotropic hypogonadism. The steroid profiles suggest that they have 17 alpha-hydroxylase deficiency. In contrast to the classical biochemical findings in 17 alpha-hydroxylase deficiency, both of these patients have hyperaldosteronism. Thus this report describes a new variant of 17 alpha-hydroxylase deficiency with hyperaldosteronism. Dexamethasone suppressed the mineralocorticoid excess, including aldosterone, and improved their hypertension. In the untreated state, ACTH, instead of the renin-angiotensin system, regulated plasma aldosterone levels, but during dexamethasone treatment the renin-angiotensin system regulated these levels.

摘要

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