抄録
The case of a 16-year-old patient with incomplete testicular feminization syndrome is reported. The patient had phenotypically female genitalia except for clitoromegaly. Hormonal examinations revealed low plasma testosterone levels but a normal concentration of 5α-dihydrotestosterone, and radiological and surgical examinations revealed no development of Müllerian structures including the uterus and the adnexa. This happened in a family with a frequent occurrence of both hypospadias and cryptorchism.
本文言語 | 英語 |
---|---|
ページ(範囲) | 101-103 |
ページ数 | 3 |
ジャーナル | Urologia Internationalis |
巻 | 46 |
号 | 1 |
DOI | |
出版ステータス | 出版済み - 1991 |
!!!All Science Journal Classification (ASJC) codes
- 泌尿器学