CONGENITAL ADRENAL HYPERPLASIA AND VANISHING TESTIS: RARE CASE OF MALE PSEUDOHERMAPHRODITISM

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

GHANEI AZAM; MOHAMMADZADE GOLNAZ; ZAREPUR EHSAN; SOHEYLIKHAH SEDIGHEH

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

Journal Paper

Paper Information

Journal: International Journal of Reproductive BioMedicine Year:2016 | Volume:14 | Issue:3 Page(s): 213-216

Download Full-Text

View:

387

Download:

106

Cites:

Information Journal Paper

Title

CONGENITAL ADRENAL HYPERPLASIA AND VANISHING TESTIS: RARE CASE OF MALE PSEUDOHERMAPHRODITISM

Author(s)

GHANEI AZAM | MOHAMMADZADE GOLNAZ | ZAREPUR EHSAN | SOHEYLIKHAH SEDIGHEH | Issue Writer Certificate

Keywords

CONGENITAL ADRENAL HYPERPLASIA

VANISHING TESTES

AMBIGUOUS GENITALIA

Abstract

Background: CONGENITAL ADRENAL HYPERPLASIA (CAH) and VANISHING TESTES are uncommon diseases that can result from hormonal and mechanical factors. Classic CAH is determined by AMBIGUOUS GENITALIA and increase in amount of 17-Hydroxyprogesterone. Simultaneous occurrence of CAH and VANISHING TESTES is a rare condition.Case: A 22-year-old boy, known case of CAH who was diagnosed as female pseudohermaphroditism due to AMBIGUOUS GENITALIA, was referred to Shahid Sadoughi Hospital, Yazd, Iran with colicky abdominal pain and hematuria. Ultrasonography has been performed and prostate tissue was reported. Karyotyping was done because of uncertainty in primary diagnosis, which revealed 46XY. For finding location of testes, ultrasonography and MRI were done and nothing was found in abdomen, inguinal canal or scrotum. Inhibin B serum level was measured to find out whether testis tissue was present in the body, which was<1 pg/ml and vanishing testis was confirmed.Conclusion: Early diagnosis and treatment are essential to prevent further sequels and karyotyping for all patients with CAH is recommended. Lifelong treatment with synthetic glucocorticoid replacement is necessary.

Cites

No record.

References

No record.

Cite

APA: Copy

GHANEI, AZAM, MOHAMMADZADE, GOLNAZ, ZAREPUR, EHSAN, & SOHEYLIKHAH, SEDIGHEH. (2016). CONGENITAL ADRENAL HYPERPLASIA AND VANISHING TESTIS: RARE CASE OF MALE PSEUDOHERMAPHRODITISM. INTERNATIONAL JOURNAL OF REPRODUCTIVE BIOMEDICINE (IRANIAN JOURNAL OF REPRODUCTIVE MEDICINE), 14(3), 213-216. SID. https://sid.ir/paper/296243/en

Vancouver: Copy

GHANEI AZAM, MOHAMMADZADE GOLNAZ, ZAREPUR EHSAN, SOHEYLIKHAH SEDIGHEH. CONGENITAL ADRENAL HYPERPLASIA AND VANISHING TESTIS: RARE CASE OF MALE PSEUDOHERMAPHRODITISM. INTERNATIONAL JOURNAL OF REPRODUCTIVE BIOMEDICINE (IRANIAN JOURNAL OF REPRODUCTIVE MEDICINE)[Internet]. 2016;14(3):213-216. Available from: https://sid.ir/paper/296243/en

IEEE: Copy

AZAM GHANEI, GOLNAZ MOHAMMADZADE, EHSAN ZAREPUR, and SEDIGHEH SOHEYLIKHAH, “CONGENITAL ADRENAL HYPERPLASIA AND VANISHING TESTIS: RARE CASE OF MALE PSEUDOHERMAPHRODITISM,” INTERNATIONAL JOURNAL OF REPRODUCTIVE BIOMEDICINE (IRANIAN JOURNAL OF REPRODUCTIVE MEDICINE), vol. 14, no. 3, pp. 213–216, 2016, [Online]. Available: https://sid.ir/paper/296243/en

Related Journal Papers

No record.

Related Seminar Papers

No record.

Related Plans

No record.

Recommended Workshops