Harlequin ichthyosis: Case report

Harlequin ichthyosis: Case report

Harlequin fetus is a rare and the most severe form of the congenital ichthyosis with an autosomal recessive inheritance. Incidence of the disease is nearly 1 in 3,00,000 live births. The disease might be lethal at birth and the affected babies are often premature. Harlequin ichthyosis (HI) is marked...

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Bibliographic Details
Main Authors: Shahrbanoo Salehin, Ahmad Azizimoghadam, Abdolghani Abdollahimohammad, Mohammad Babaeipour-Divshali
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Journal of Research in Medical Sciences
Subjects:
ABCA12 gene mutation
autosomal recessive
skin abnormalities
Online Access:http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2013;volume=18;issue=11;spage=1004;epage=1005;aulast=Salehin

Internet

http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2013;volume=18;issue=11;spage=1004;epage=1005;aulast=Salehin

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