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Information Journal Paper

Title

TESTICULAR FEMINIZATION: REPORT OF THREE CASES IN A FAMILY

Pages

  6-8

Abstract

 Cases of the complete syndrome of testicular feminization were reported early in the 19th century, but it was in 1950 that Lawson recognized the etiology in a patient with amenorrhoea and failing pubic and axillary hair, which was unresponsive to testesterone therapy. The prevalence of androgen resistance is estimated to be between 1:20.000 and 1:64.000 men and the complete form is the third most common cause of PRIMARY AMENORRHEA. Testicular feminization is transmitted as X-linked recessive trait. In this article, we report on three siblings in a family with complete form of androgen insensitivity. The first case, the youngest of the siblings, was recognized by an INGUINAL HERNIA operation.The diagnosis was established by chromosomal analysis, hormonal assays, sonography, and pathological examination after laparatomy.

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  • Cite

    APA: Copy

    MOAYERI, H.. (2003). TESTICULAR FEMINIZATION: REPORT OF THREE CASES IN A FAMILY. IRANIAN JOURNAL OF PEDIATRICS, 12(4), 6-8. SID. https://sid.ir/paper/75868/en

    Vancouver: Copy

    MOAYERI H.. TESTICULAR FEMINIZATION: REPORT OF THREE CASES IN A FAMILY. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2003;12(4):6-8. Available from: https://sid.ir/paper/75868/en

    IEEE: Copy

    H. MOAYERI, “TESTICULAR FEMINIZATION: REPORT OF THREE CASES IN A FAMILY,” IRANIAN JOURNAL OF PEDIATRICS, vol. 12, no. 4, pp. 6–8, 2003, [Online]. Available: https://sid.ir/paper/75868/en

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