Addison W A, Hammond C B, Tyrey L, Schomberg D W
Obstet Gynecol. 1976 Mar;47(3):331-6.
Two siblings are presented, both with classic androgen-insensitivity syndrome (AIS). Endocrine testing was carried out and then gonadectomy was performed. Studies in these patients with AIS revealed low control serum FSH. In these patients serum FSH was not significantly suppressed by intravenous estrogen nor adequately stimulated by FSH-LH-releasing hormone but rose normally after castration. The various studies are interpreted in the light of the known kinetics of pituitary gonadotorpins and their modulation by gonadal steroids. A third sibling is also presented.
介绍了两名患有典型雄激素不敏感综合征(AIS)的兄弟姐妹。进行了内分泌检测,然后实施了性腺切除术。对这些AIS患者的研究显示,血清促卵泡激素(FSH)的控制水平较低。在这些患者中,静脉注射雌激素并未显著抑制血清FSH,促性腺激素释放激素也未对其产生充分刺激,但去势后血清FSH正常升高。根据已知的垂体促性腺激素动力学及其受性腺类固醇调节的情况对各项研究进行了解释。还介绍了第三名兄弟姐妹。