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Congenital adrenal hyperplasia in a 66-year-old female

A D Wright, T C Harvey, G Holder

Postgraduate Medical Journal

|May 1, 1981

Abstract:

A 66-year-old genotypically female patient was reared as a man. Investigations showed a partial adrenal 21-hydroxylase deficiency, and pituitary gonadotrophin secretion typical of a post-menopausal woman.

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