Leroith D, Farkash Y, Bar-Ziev J, Spitz I M
Isr J Med Sci. 1980 Jul;16(7):514-8.
Four siblings with classic Bardet-Biedl syndrome were studied. The brother had hypogonadism of testiculr origin, with high gonadotropin levels and exaggerated responses to luteinizing-hormone-releasing hormone, whereas the three sisters showed a normal hypothalamic-pituitary-gonadal axis. The remaining pituitary hormone function was intact.
对四名患有典型巴德-比德尔综合征的兄弟姐妹进行了研究。该名兄弟患有睾丸源性性腺功能减退，促性腺激素水平较高，对促黄体生成素释放激素反应过度，而三名姐妹的下丘脑-垂体-性腺轴功能正常。其余垂体激素功能完好。
