Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein-1 mutation: A case report.
Kevin KoschitzkiBernadett KurzJulia SchremlJudith FischerAlrun HotzChristoph M HammersMark BerneburgDennis NiebelStephan SchremlPublished in: Clinical case reports (2024)
. Despite increased understanding, effective treatment options for PPK, including SPPK-I, remain limited.
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