Wortsman J, Hansen M, Kousseff B G, Hamidinia A
Fertil Steril. 1982 Jan;37(1):123-5. doi: 10.1016/s0015-0282(16)45991-1.
We have reported a sibship in which all three males had azoospermia and a normal 46,XY karyotype. The mechanisms for the production of azoospermia were Kallmann's syndrome and bilateral agenesis of the globus major (head of the epididymis) in the proband and bilateral agenesis of the vasa deferentia and seminal vesicles in the two brothers. It is suggested that this syndrome of agenesis of the testicular excretory system may be a variant of Kallmann's syndrome.
我们报道了一个家系，其中所有三名男性均患有无精子症且核型为正常的46,XY。先证者无精子症的病因是卡尔曼综合征和双侧附睾头缺失，而两名兄弟的病因是双侧输精管和精囊缺失。有人提出，这种睾丸排泄系统发育不全综合征可能是卡尔曼综合征的一种变体。
