Vague J, Guidon J
Sem Hop. 1977 Nov 9;53(38):2125-33.
The cause of male pseudohermaphroditism : polydystrophy, gonadal dysplasia, agenesis or precocious abiotrophy of Leydig cells, defect of testicular stimulation by foetal hypophysis, testosterone, biosynthesis abnormalities 5 varieties of which are identified, 5 alpha reductase defect, testosterone or dihydrotestosterone insenstivity complete and incomplete forms, defect of secretion or action of Mullerian ducts inhibitor can be found in the majority of cases by clinical and para-clinical analysis. Practical management results from this diagnosis.
多系统发育异常、性腺发育不全、Leydig细胞发育不全或过早退变、胎儿垂体对睾丸刺激的缺陷、睾酮生物合成异常(已确定5种类型)、5α还原酶缺陷、睾酮或双氢睾酮完全和不完全性不敏感、苗勒管抑制物分泌或作用缺陷,多数情况下通过临床和辅助临床分析可发现这些病因。基于此诊断进行实际处理。