Volume 12, Issue 45 (6-2005)                   RJMS 2005, 12(45): 43-48 | Back to browse issues page

XML Persian Abstract Print


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

Basiri B, Shokoohi M. A Case Report of Two Siblings with Harlequin Ichthyosis . RJMS 2005; 12 (45) :43-48
URL: http://rjms.iums.ac.ir/article-1-429-en.html
Abstract:   (18207 Views)

    Harlequin Ichthyosis (HI) describes a severe erythrodermic ichthyosis and causes a distinctive and grotesque appearance at birth. Survival is now possible therefore, harlequin ichthyosis is a more appropriate term than harlequin fetus. Incidence is 1 in 300,000 births. An autosomal recessive pattern of inheritance is seen in this disorder, but a new autosomal dominant mutation may possibly be responsible. The prognosis is ominous and most of the affected neonates die in the first hours or days of life. In this case report we present two cases of HI who were the first and the second baby of a family and their parents were cousins.

Full-Text [PDF 292 kb]   (7431 Downloads)    
Type of Study: case report | Subject: Pediatric Disease

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