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A de novo mutation of KRT1 in a baby girl causing epidermolytic ichthyosis with impressive epidermolytic palmoplantar keratoderma.

Dermatology online journal - 15 Jul 2020

Calì Francesco, Failla Pinella, Vinci Mirella, Siragusa Maddalena, Schepis Carmelo

Abstract excerpt

We report a 6-year-old girl showing epidermolytic ichthyosis/epidermolytic hyperkeratosis (EI/EH). Targeted Next Generation Sequencing revealed a de novo, previously unidentified KRT1 mutation. The findings of this study expands the clinical and spectrum and genotype-phenotype correlation associated with EI/EH.

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PMID: 32898404

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