Volume 36, Number 2 (7-2012)                   Research in Medicine 2012, 36(2): 114-116 | Back to browse issues page


XML Persian Abstract Print


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

Kazemi Z, Noori Rahmatabadi N. A rare case of Harlequin Ichthyosis born in Zabol hospital, Iran. Research in Medicine. 2012; 36 (2) :114-116
URL: http://pejouhesh.sbmu.ac.ir/article-1-1048-en.html

Department of Gynecology and Obstetrics, Zabol University of Medical Sciences, Zabol, Iran , medicalopto@yahoo.com
Abstract:   (4846 Views)
Abstract Background: Harlequin ichthyosis is a fatal and extremely rare disorder it is an inborn error of epidermal keratinisation with autosomal recessive inheritance. In most cases, neonates die within a few days after birth. Case presentation: We describe a male term infant born from a 32 years old woman with odd looking, clown like face. The skin was composed of rigid fixed plaques separated by deep red fissures ears and eyes were not developed. Despite vigorous attempts at resuscitation he died within a few minutes. Conclusion: As ichthyosis is autosomal recessive, genetic counseling and prenatal screening is important. Keywords: Harlequin ichthyosis, Eclabiom, Ectropion
Full-Text [PDF 112 kb]   (1541 Downloads)    
Type of Study: Case report |
Received: 2012/10/20

Send email to the article author


Creative Commons License
This Journal is licensed under a Creative Commons Attribution 4.0 International License  | Research in Medicine

Designed & Developed by : Yektaweb