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

Persian Verion

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

video

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

sound

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

Persian Version

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

View:

1,513
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

COMPLETE ANDROGEN INSENSITIVITY SYNDROME (CAIS) (CASE REPORT)

Pages

  147-149

Abstract

 Complete androgen insensitivity syndrome is characterized by normal FEMALE appearance, including external genitalia in the presence of a 46 xy karyotype. CAIS is a rare disorder, the prevalence is estimated at between 1 in 20000 and 1 in 60000 live births. However, this condition is found more frequently in the subpopulation of girls with inguinal hernias, and the incidence of CAIS has estimated to be 0.8% to 2.4% in girls with inguinal hernias. In this article two cases of CAIS have been reported.Case 1: An 18 years old girl with chief complains of primary amenorrhea, in physical examination bilateral palpable testes in inguinal areas. Ultrasonography revealed the absence of uterus, fallopian tubes and proximal vagina. She had a 46 xy karyotype. After consultation, she underwent bilateral orchiectomy and reared as FEMALE.Case 2: A 16 years old boy that had reared FEMALE in neonatal period, but after bilateral inguinal herniorrhaphy, five years later she reared as male. After puberty and secondary sexual development this misguided boy underwent bilateral mastectomy and he encountered with some psychosocial problems.CAIS results in total feminization and the FEMALE role should be supported with postpubertal orchiectomy to avoid the risk of malignancy.

Multimedia

  • No record.
  • Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    NOURI ZADEH, D., & HASHEM ZADEH, SH.. (2008). COMPLETE ANDROGEN INSENSITIVITY SYNDROME (CAIS) (CASE REPORT). MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, 30(1), 147-149. SID. https://sid.ir/paper/46855/en

    Vancouver: Copy

    NOURI ZADEH D., HASHEM ZADEH SH.. COMPLETE ANDROGEN INSENSITIVITY SYNDROME (CAIS) (CASE REPORT). MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2008;30(1):147-149. Available from: https://sid.ir/paper/46855/en

    IEEE: Copy

    D. NOURI ZADEH, and SH. HASHEM ZADEH, “COMPLETE ANDROGEN INSENSITIVITY SYNDROME (CAIS) (CASE REPORT),” MEDICAL JOURNAL OF TABRIZ UNIVERSITY OF MEDICAL SCIENCES, vol. 30, no. 1, pp. 147–149, 2008, [Online]. Available: https://sid.ir/paper/46855/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button