Harlequin ichthyosis: a case report
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Case Report
P: 52-54
March 2007

Harlequin ichthyosis: a case report

Gulhane Med J 2007;49(1):52-54
1. Sağlık Bakanlığı Ankara Eğitim ve Araştırma Hastanesi Çocuk Sağlığı ve Hastalıkları Kliniği, Ankara
2. Sağlık Bakanlığı Ankara Eğitim ve Araştırma Hastanesi, Patoloji Kliniği, Ankara
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Received Date: 12.07.2006
Accepted Date: 27.11.2006
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ABSTRACT

Harlequin ichthyosis represents the most severe form of nonbullous ichthyosis. It is inherited in an autosomal recessive pattern and very rare. This disease destroys the skin's barrier system and severe cutaneous infections develop in affected newborns. Malformations of ears and nose, and hypoplasia of fingers and nails are seen. It is usually lethal in the neonatal period. A case of Harlequin ichthyosis is herein reported and discussed.

Keywords:
Harlequin ichthyosis, keratinization disorders, newborn