Garty B, Shuper A, Mimouni M, Varsano I, Kauli R
Eur J Pediatr. 1982 Nov;139(3):201-3. doi: 10.1007/BF01377358.
A 7-year-old boy with Prader-Labhart-Willi syndrome who had precocious adrenarche was found to have primary gonadal failure, as evidenced by appropriate laboratory investigations: elevated basal levels of plasma FSH and LH with exaggerated responses to LH-RH stimulation and unresponsiveness of plasma testosterone to repeated hCG stimulations. The elevated values of plasma DHEA which were found indicate an early activation of the adrenal gland. This patient demonstrates the variability of pubertal development in the Prader-Labhart-Willi syndrome, with the unusual association of primary gonadal failure and precocious adrenarche.
一名患有普拉德-威利综合征且有肾上腺功能初现早熟的7岁男孩,经适当实验室检查发现存在原发性性腺功能减退:血浆促卵泡生成素(FSH)和促黄体生成素(LH)基础水平升高,对促黄体生成素释放激素(LH-RH)刺激反应过度,血浆睾酮对重复的人绒毛膜促性腺激素(hCG)刺激无反应。所发现的血浆脱氢表雄酮(DHEA)值升高表明肾上腺早期激活。该患者显示了普拉德-威利综合征青春期发育的变异性,伴有原发性性腺功能减退和肾上腺功能初现早熟的不寻常关联。