Volume 1, Issue 1 (winter 2013)                   Clin Exc 2013, 1(1): 131-140 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

karami H, Mohammadjafari H, Alam A, Ghassemi M, Taghipoor M, Sharifian R. Bilateral wilms tumor with anidria, hypospadias and mental retardation (WAGR syndrome): A case report. Clin Exc 2013; 1 (1) :131-140
URL: http://ce.mazums.ac.ir/article-1-32-en.html
Abstract:   (10959 Views)

Wilms tumor is the most common renal tumor of childhood that in 1, 27. Of cases is along with congenital anomalies such as anidria, genitourinary abnormalities and mental retardation. A 3.5 years old child was treated with the diagnosis of wilms tumor. He also had bilateral anidria, hypospadiasis and mental retardation. There were no other congenital abnormalities. The patient was taken under operation and chemotherapy was started for him. Now the patient is in the second phase of chemotherapy and the treatment has been successful until now.

Full-Text [PDF 605 kb]   (7412 Downloads)    
Subject: اپيدميولوژي
Received: 2013/01/13 | Accepted: 2013/08/27 | Published: 2013/08/27

Add your comments about this article : Your username or Email:
CAPTCHA

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 4.0 | Clinical Excellence

Designed & Developed by : Yektaweb