Harlequin ichthyosis: A case report and literature review

Abstract

Abstract Harlequin ichthyosis is a rare autosomal recessive disorder occurring in 1: 3,000,000 birth characterized by thick keratin skin with a scaly appearance. Preterm deliveries, early, and consanguinity of marriage are some risk factors. Antenatal checkup of DNA for ABCA12 mutation helps in diagnosis but ultrasonography in places was not available.

Keywords

• ABCA12 mutation
• genetic disorder
• harlequin ichthyosis
• ichthyosis congenital