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In this study, a genetic analysis identified a pathogenic variant in the ALOXE3 gene associated with non-bullous congenital ichthyosiform erythroderma, and the patient's response to antifungal treatment highlights the risk of cutaneous fungal infections.

This review discusses changes in keratin structure or gene expression that result in various skin disorders and reports no new clinical findings.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.