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Congenital adrenal hyperplasia in a 66-year-old female.
  1. A. D. Wright,
  2. T. C. Harvey,
  3. G. Holder,
  4. D. C. Anderson,
  5. B. T. Rudd


    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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