Syndromic Epidermolysis Bullosa Simplex Subtype Due to Mutations in the KLHL24 Gene: Series of Case Reports in Russian Families

    July 2024 in “ Frontiers in Medicine
    Y. Y. Kotalevskaya, В. А. Степанов
    Studysummary This study reports that analyzing the clinical manifestations of different genetic variants in EBS families helps predict disease progression and severity, guide complication risk assessment, and plan necessary medical care.
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