مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

COMPLETE ANDROGEN INSENSITIVITY SYNDROME IN THREE SISTERS (CASE REPORT)

Pages

  353-356

Abstract

 Disorders of sexual development (DSD) are congenital anomalies due to atypical development of chromosomes, gonads and anatomy. Complete androgen insensitivity syndrome (CAIS), also known as testicular feminization (TF) is a rare DSD disease. The majority of CAIS patients apply to hospital with the complaint of primary amenorrhea or INFERTILITY. Given that CAIS patients are all phenotypically female while having 46, XY karyotypes, CAIS diagnosis should be disclosed in an age-appropriate manner preferably by a mental health professional. Cases are reported here for three 46XY siblings consistent with CAIS.

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    APA: Copy

    VERIM, LEVENT. (2014). COMPLETE ANDROGEN INSENSITIVITY SYNDROME IN THREE SISTERS (CASE REPORT). INTERNATIONAL JOURNAL OF FERTILITY AND STERILITY, 7(4), 353-356. SID. https://sid.ir/paper/305434/en

    Vancouver: Copy

    VERIM LEVENT. COMPLETE ANDROGEN INSENSITIVITY SYNDROME IN THREE SISTERS (CASE REPORT). INTERNATIONAL JOURNAL OF FERTILITY AND STERILITY[Internet]. 2014;7(4):353-356. Available from: https://sid.ir/paper/305434/en

    IEEE: Copy

    LEVENT VERIM, “COMPLETE ANDROGEN INSENSITIVITY SYNDROME IN THREE SISTERS (CASE REPORT),” INTERNATIONAL JOURNAL OF FERTILITY AND STERILITY, vol. 7, no. 4, pp. 353–356, 2014, [Online]. Available: https://sid.ir/paper/305434/en

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