Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein‐1 mutation: A case report

URN to cite this document:: urn:nbn:de:bvb:355-epub-586199
DOI to cite this document:: 10.5283/epub.58619

Koschitzki, Kevin

; Kurz, Bernadett ; Schreml, Julia ; Fischer, Judith ; Hotz, Alrun ; Hammers, Christoph M. ; Berneburg, Mark

; Niebel, Dennis

; Schreml, Stephan

License: Creative Commons Attribution Non-commercial No Derivatives 4.0
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Date of publication of this fulltext: 13 Jul 2024 09:01

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Abstract

Keratosis palmoplantaris striata type I (SPPK-I) is a rare autosomal-dominant type of hereditary epidermolytic palmoplantar keratoderma, which can be caused by mutations in desmoglein-1 (DSG-1). Patients suffer from hyperkeratotic plaques and painful palmoplantar fissures. Unfortunately, treatment options including salicylic vaseline, topical corticosteroids, phototherapy, and retinoids are ...