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

Research output: Contribution to journalArticle

Abstract

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.

Original languageEnglish
JournalDermatology Online Journal
Volume26
Issue number7
Publication statusPublished - Jul 15 2020

ASJC Scopus subject areas

  • Dermatology

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