Vanelli M, Bernasconi S, Caronna N, Virdis R, Terzi C, Giovannelli G
Helv Paediatr Acta. 1984 Oct;39(4):373-7.
True precocious puberty is reported in a male child with Prader-Labhart-Willi syndrome. The diagnosis of precocious puberty was made at 8 6/12 years of age when a spontaneous migration of previously unpalpable testes (mean volume = 5 ml), an increase in penis length (from 2 to 6 cm) and a growth spurt (8.4 cm/year) occurred. The follow-up until 13 years of age (bone age 15 years) showed a progressive pubertal development, facial acne (10 years), frequent spontaneous erections and ejaculations (11 years). Repeated endocrine and neuroradiological investigations were consistent with an idiopathic form of precocious puberty.
一名患有普拉德-威利综合征的男童被报道出现真性性早熟。该患儿在8岁6个月时被诊断为性早熟,当时原本无法触及的睾丸自发下降(平均体积 = 5毫升),阴茎长度增加(从2厘米增至6厘米),并出现生长加速(每年8.4厘米)。随访至13岁(骨龄15岁)显示青春期发育持续进展,10岁时出现面部痤疮,11岁时频繁出现自发勃起和射精。反复进行的内分泌和神经放射学检查结果符合特发性性早熟的表现。