Epidermolytic ichthyosis: Clinical spectrum and burden of disease in a large German cohort. [PDF]
J Eur Acad Dermatol VenereolBackground Keratinopathic ichthyoses are a group of hereditary skin disorders caused by pathogenic variants in keratin genes such as KRT1, KRT2 and KRT10, resulting in conditions such as epidermolytic ichthyosis (EI), autosomal-recessive EI, superficial
Frommherz L +11 more
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Epidermolytic hyperkeratosis in inflammatory linear verrucous epidermal nevus
Indian Journal of Dermatology, 2011 Epidermolytic hyperkeratosis presents with perinuclear vacuolization of the keratinocytes in spinous and granular layers, keratinocytes with ill-defined limits, which leads to a reticulate appearance of the epidermis, an increased number of variously ...
Naser Tayyebi Meibodi +2 more
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Superficial Epidermolytic Ichthyosis: Clinical and Histopathological Features in Two Siblings
Nepal Journal of Dermatology, Venereology & LeprologySuperficial epidermolytic ichthyosis (SEI), a type of keratinopathic ichthyosis (KPI) caused by mutations in the K2e gene, is clinically characterized by superficial blistering, hyperkeratosis predominantly involving flexures and joints, Mauserung ...
Pooja Shah, Bela Padhiar
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Incidental Cutaneous Reaction Patterns: Epidermolytic Hyperkeratosis, Acantholytic Dyskeratosis, and Hailey-Hailey-Like Acantholysis: A Potential Marker of Premalignant Skin Change [PDF]
Journal of Skin Cancer, 2011 Focal acantholytic dyskeratosis (FAD), epidermolytic hyperkeratosis (EHK), and Hailey-Hailey-like acantholysis (HH) represent unique histology reaction patterns, which can be associated with defined phenotypic and genotypic alterations.
Erich M. Gaertner
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Epidermolytic hyperkeratosis: clinical update
Clinical, Cosmetic and Investigational Dermatology, 2019 Denice Peter Rout,* Anushka Nair,* Anand Gupta, Piyush KumarAmity Institute of Biotechnology, Amity University Mumbai, Navi Mumbai, India*These authors contributed equally to this workAbstract: Epidermolytic hyperkeratosis (EHK), earlier termed as ...
Peter Rout D, Nair A, Gupta A, Kumar P
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Epidermolytic hyperkeratosis of the vulva: Case report and review of the literature [PDF]
Skin Health and DiseaseEpidermolytic hyperkeratosis is a rare histopathological phenomenon which has been reported in a number of dermatological conditions. It is rare but can cause chronic and intractable symptoms which can impede the quality of life of those affected ...
Dilshad Sachedina +3 more
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Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein‐1 mutation: A case report [PDF]
Clinical Case ReportsKey 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).
Kevin Koschitzki +8 more
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ALOXE3 missense variant in a Chihuahua with autosomal recessive ichthyosis. [PDF]
Anim GenetAbstract Ichthyoses are a heterogenous group of inherited disorders that are characterized by excessive scale formation on the skin. We investigated a Chihuahua with severe scaling since age 12 weeks. The scaling was generalized and involved the entire body and legs. The paw pads were mildly hyperkeratotic.
Vinberg C +5 more
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Congenital Segmental Erosions and Hyperkeratotic Plaques in a Male Infant: A Quiz [PDF]
Acta Dermato-VenereologicaKaan Yilmaz +4 more
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Epidermolytic ichthyosis: New insights and ongoing challenges. [PDF]
J Eur Acad Dermatol VenereolJournal of the European Academy of Dermatology and Venereology, Volume 39, Issue 5, Page 893-894, May 2025.
Mazereeuw-Hautier J.
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