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:

230
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

160
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

A female with 46, XY Disorder of Sexual Development with normal SRY gene sequence: A case report

Pages

  14-21

Abstract

 Background and objectives: Disorders of sex development (DSD) are a medical condition that affects the normal process of sexual development. Various of the genes needed for gonad development have been identified by investigation of patients with disorders sex development (DSD). Phenotypes of patients with 46, XY DSD range from agonadism in female phenotype with complete external genitalia to male phenotype with testicular regression. Individuals with 46, XYagonadiam show a wide range of clinical features and in some cases, there is not a clear diagnosis for these patients. We presented the clinical and molecular study a patient with 46, XY female without gonadal tissue. Case presentation: A 27-year-old female was attended to our center because of primary amenorrhea. Ultrasonography did not show gonadal tissue including Mullerian structures, uterus, and Wolffian structures. Also, the patient had not streak gonad. We performed cytogenetic study and molecular analysis, including automated sequencing of the entire coding region of SRY gene, in the patient with agonadism. Our result showed 46, XY karyotype. Also, we noticed that molecular mutations in SRY are not identified as a cause of DSD female without a gonadal tissue. Laboratory examination showed that this case is a unique patient with 46, XYfemale agonadism that has no association with previously described. Conclusion: The present case was a patient with 46, XYagonadism without hormonal or kidney defect and we did not detect mutation in SRY gene. To our knowledge, this case is a unique patient with 46, XYagonadism that has no association with previously described. So this case would be helpful for clinicians to assess 46, XY female patients without gonadal tissue.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    Agha Gholizadeh, Mehdi, bazgir, Afsaneh, SARVAR, FAEZEH, & PAKZAD, ZAHRA. (2019). A female with 46, XY Disorder of Sexual Development with normal SRY gene sequence: A case report. JORJANI BIOMEDICINE JOURNAL, 7(1), 14-21. SID. https://sid.ir/paper/724532/en

    Vancouver: Copy

    Agha Gholizadeh Mehdi, bazgir Afsaneh, SARVAR FAEZEH, PAKZAD ZAHRA. A female with 46, XY Disorder of Sexual Development with normal SRY gene sequence: A case report. JORJANI BIOMEDICINE JOURNAL[Internet]. 2019;7(1):14-21. Available from: https://sid.ir/paper/724532/en

    IEEE: Copy

    Mehdi Agha Gholizadeh, Afsaneh bazgir, FAEZEH SARVAR, and ZAHRA PAKZAD, “A female with 46, XY Disorder of Sexual Development with normal SRY gene sequence: A case report,” JORJANI BIOMEDICINE JOURNAL, vol. 7, no. 1, pp. 14–21, 2019, [Online]. Available: https://sid.ir/paper/724532/en

    Related Journal Papers

  • No record.
  • 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