Retinoid Therapy in a Case of Harlequin Ichthyosis with a Short Literature Review

Retinoid Therapy in a Case of Harlequin Ichthyosis with a Short Literature Review

Harlequin ichthyosis (HI) is a genetically inherited epidermal disorder due to the mutation of the ABCA12 gene, which is responsible for lipid transportation, and presents with large keratinised scales characterised by deep erythematous fissures, with ectropion and eclabium. A moderate number of cas...

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Bibliographic Details
Main Authors: Emad Bahashwan, Jaber Alfaifi, Sahar Elmaghawri Mohamed Moursi, Youssef Elbayoumi Soliman
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Case Reports in Dermatological Medicine
Online Access:http://dx.doi.org/10.1155/2024/8729318
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