Volume 14, Issue 54 (4-2007)                   RJMS 2007, 14(54): 17-20 | Back to browse issues page

XML Persian Abstract Print


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

Ehsanipour F. Cornelia De Lange Syndrome: A Case Report . RJMS 2007; 14 (54) :17-20
URL: http://rjms.iums.ac.ir/article-1-694-en.html
Abstract:   (7558 Views)

    Introduction: Cornelia de lange syndrome(CDLS) is a rare syndrome which is characterized by multiple congenital anomalies, mental retardation, characteristic facial appearance, developmental delay, skeletal malformation, hirsutism, and various ophthalmologic problems. The diagnosis of this syndrome is clinical. Case Report: The patient of the present case report was an infant with cornelia de lange syndrome. Conclusion: An increased awareness of this syndrome may result in an early diagnosis and a decrease in morbidity.

Full-Text [PDF 127 kb]   (3041 Downloads)    
Type of Study: case report | Subject: Pediatric Infectious

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 | Razi Journal of Medical Sciences

Designed & Developed by : Yektaweb