ArticleClinical case reports2024
Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein-1 mutation: A case report.
Article in Clinical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Ectodermal dysplasias and isolated ectodermal anomalies: expanding the clinical and molecular spectrum in a cohort of 36 patients.European journal of pediatrics · 2025Article
- Atypical manifestation of psoriasis in the elderly: possible expression of Mal de Meleda diagnosis review and case report.Frontiers in medicine · 2025Article
- Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein-1 mutation: A case report.Clinical case reports · 2024Article
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Authors and funding
9 authors.
Funding
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Abstract
Key Clinical Message: 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 inefficient. Abstract: Hereditary palmoplantar keratodermas (PPKs) represent a heterogeneous group of rare skin disorders with epidermal palmoplantar hyperkeratosis. Mutations in the
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