Wright A D, Harvey T C, Holder G, Anderson D C, Rudd B T
Postgrad Med J. 1981 May;57(667):317-20. doi: 10.1136/pgmj.57.667.317.
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.
一名66岁的基因型女性患者自幼被当作男性抚养。检查发现其存在部分肾上腺21-羟化酶缺乏,以及绝经后女性典型的垂体促性腺激素分泌情况。