Mark E, Castells S, Glassberg K, Choi S J, Tolete-Velcek F, David K, Migeon C J
Urology. 1983 Feb;21(2):168-71. doi: 10.1016/0090-4295(83)90017-1.
A diagnosis of androgen receptor deficiency was made in a male with ambiguous genitalia during the neonatal period. Since the neonate had a small hypospadiac phallus with laboratory evidence of a receptor deficiency and clinical unresponsiveness to high levels of androgen, it was decided to assign a female gender. Bilateral orchiectomy and phallic recession were performed.
一名患有生殖器模糊的男性新生儿被诊断为雄激素受体缺乏症。由于该新生儿有一个小的尿道下裂阴茎，实验室检查有受体缺乏的证据，且对高水平雄激素临床无反应，因此决定将其性别指定为女性。进行了双侧睾丸切除术和阴茎退缩术。
