Zipf W B, Kelch R P, Bacon G E
Clin Genet. 1977 Apr;11(4):249-54. doi: 10.1111/j.1399-0004.1977.tb01309.x.
Two half-brothers with short stature secondary to growth hormone deficiency and a family history implicating X-linked transmission were studied extensively for other endocrine abnormalities. The proband had a normal physical examination, except for small stature and small external genitalia. ACTH and TSH release were normal. LH and FSH responses during an i.v. GnRH test were severely blunted. His half-brother also had a normal physical examination, except for severe short stature and very small external genitalia. Deficiencies of ACTH, and TSH as well as GH were documented. An i.v. GnRH test showed no LH or FSH response. These studies support the existence of an X-linked recessive form of hypopituitarism and portend the clinical usefulness of the i.v. GnRH test in evaluating gonadotropin reserve.
对两名同父异母兄弟进行了广泛研究,他们因生长激素缺乏导致身材矮小,且家族病史提示为X连锁遗传,以查找其他内分泌异常情况。先证者体格检查正常,只是身材矮小和外生殖器较小。促肾上腺皮质激素(ACTH)和促甲状腺激素(TSH)释放正常。静脉注射促性腺激素释放激素(GnRH)试验期间,促黄体生成素(LH)和促卵泡生成素(FSH)反应严重减弱。他的同父异母兄弟体格检查也正常,只是身材严重矮小且外生殖器非常小。已证实存在促肾上腺皮质激素、促甲状腺激素以及生长激素缺乏。静脉注射GnRH试验显示无LH或FSH反应。这些研究支持存在X连锁隐性垂体功能减退症,并预示静脉注射GnRH试验在评估促性腺激素储备方面具有临床实用性。