Jaskulsky S R, Stone N N
Urology. 1987 Feb;29(2):207-8. doi: 10.1016/0090-4295(87)90155-5.
Prader-Willi syndrome is characterized by eating abnormalities, infantile hypotonia, obesity, mental retardation, and hypogonadism. The causation of hypogonadism varies. We describe a patient with Prader-Willi syndrome whose hypogonadism is secondary to a hypothalamic defect. Individualization of patients with this syndrome is suggested. Based on the particular hormonal abnormality identified, a treatment plan can be constructed. Cryptorchidism should be approached in the usual fashion.
普拉德-威利综合征的特征包括饮食异常、婴儿期肌张力减退、肥胖、智力障碍和性腺功能减退。性腺功能减退的病因各不相同。我们描述了一名患有普拉德-威利综合征的患者，其性腺功能减退继发于下丘脑缺陷。建议对该综合征患者进行个体化治疗。根据所确定的特定激素异常情况，可以制定治疗方案。隐睾症应按常规方式处理。
