Cantalamessa L, Baldini M, Ambrosi B, Fraccaro M
Cattedra di Semeiotica Medica I, Università di Milano, Italy.
Am J Med Genet. 1989 May;33(1):117-20. doi: 10.1002/ajmg.1320330117.
Two brothers referred for hypogonadism presented with short stature, mild mental retardation, and minor anomalies. In addition, both patients had hypogonadism due to primary gonadal failure and mitral valve prolapse, in the absence of other heart defects. A complete hormonal evaluation in one of the patients showed abnormal growth hormone (GH) and gonadotropin responses to different stimuli, findings suggestive of a disorder of hypothalamic-pituitary regulation. Both patients had normal chromosomes (46,XY) as did their mother (46,XX), who had some of the clinical manifestations found in her sons but in a milder form. We propose that this is a new syndrome.
两名因性腺功能减退前来就诊的兄弟身材矮小、轻度智力发育迟缓且有轻微异常。此外,两名患者均因原发性性腺功能衰竭和二尖瓣脱垂而出现性腺功能减退,且无其他心脏缺陷。对其中一名患者进行的全面激素评估显示,生长激素(GH)和促性腺激素对不同刺激的反应异常,这一结果提示下丘脑 - 垂体调节紊乱。两名患者及其母亲的染色体均正常(46,XY和46,XX),其母亲有一些在儿子身上发现的临床表现,但症状较轻。我们认为这是一种新的综合征。