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Darier and Hailey-Hailey disease: update 2021.
Rogner DF, Lammer J, Zink A, Hamm H. Rogner DF, et al. J Dtsch Dermatol Ges. 2021 Oct;19(10):1478-1501. doi: 10.1111/ddg.14619. J Dtsch Dermatol Ges. 2021. PMID: 34661345
The autosomal-dominant genodermatoses Darier disease and Hailey-Hailey disease present special challenges to dermatologists. Despite their similar pathogenesis featuring impaired adhesion of suprabasal keratinocytes as a result of defective ATPases in epiderm …
The autosomal-dominant genodermatoses Darier disease and Hailey-Hailey disease present special challenges to dermatolog …
Hailey-Hailey disease: clinical, diagnostic and therapeutic update.
Porro AM, Arai Seque C, Miyamoto D, Vanderlei Medeiros da Nóbrega D, Simões E Silva Enokihara MM, Giuli Santi C. Porro AM, et al. An Bras Dermatol. 2024 Sep-Oct;99(5):651-661. doi: 10.1016/j.abd.2023.12.003. Epub 2024 May 23. An Bras Dermatol. 2024. PMID: 38789364 Free PMC article. Review.
Hailey-Hailey disease is a rare genodermatosis described in 1939, with an autosomal dominant inheritance pattern, characterized by compromised adhesion between epidermal keratinocytes. ...
Hailey-Hailey disease is a rare genodermatosis described in 1939, with an autosomal dominant inheritance pattern, chara …
Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review.
Martina E, Diotallevi F, Radi G, Campanati A, Offidani A. Martina E, et al. Toxins (Basel). 2021 Feb 5;13(2):120. doi: 10.3390/toxins13020120. Toxins (Basel). 2021. PMID: 33562846 Free PMC article.
The best-reported evidence concerns focal idiopathic hyperhidrosis, Raynaud phenomenon, suppurative hidradenitis, Hailey-Hailey disease, epidermolysis bullosa simplex Weber-Cockayne type, Darier's disease, pachyonychia congenita, aquagenic keratoderma, alopec …
The best-reported evidence concerns focal idiopathic hyperhidrosis, Raynaud phenomenon, suppurative hidradenitis, Hailey-Hailey …
Benign Familial Pemphigus.
Adusumilli NC, Friedman AJ. Adusumilli NC, et al. JAMA Dermatol. 2022 Mar 1;158(3):315. doi: 10.1001/jamadermatol.2021.5177. JAMA Dermatol. 2022. PMID: 35019935 No abstract available.
Pumping the Breaks on Acantholytic Skin Disorders: Targeting Calcium Pumps, Desmosomes, and Downstream Signaling in Darier, Hailey-Hailey, and Grover Disease.
Harmon RM, Ayers JL, McCarthy EF, Kowalczyk AP, Green KJ, Simpson CL. Harmon RM, et al. J Invest Dermatol. 2025 Mar;145(3):494-508. doi: 10.1016/j.jid.2024.06.1289. Epub 2024 Aug 29. J Invest Dermatol. 2025. PMID: 39207315 Review.
However, genetic acantholytic disorders originate from more indirect mechanisms. Darier disease and Hailey-Hailey disease arise from mutations in the endoplasmic reticulum calcium pump, SERCA2, and the Golgi calcium/manganese pump, SPCA1, respectively. ...
However, genetic acantholytic disorders originate from more indirect mechanisms. Darier disease and Hailey-Hailey disease …
Herpetic infection in Hailey-Hailey disease.
Lim S, O'Connell KA, Pariser RJ. Lim S, et al. Dermatol Online J. 2023 Feb 15;29(1). doi: 10.5070/D329160227. Dermatol Online J. 2023. PMID: 37040924 Free article. No abstract available.
Nonsyndromic epidermal differentiation disorders: a new classification toward pathogenesis-based therapy.
Akiyama M, Choate K, Hernández-Martín Á, Aldwin-Easton M, Bodemer C, Gostyński A, Hovnanian A, Ishida-Yamamoto A, Malovitski K, O'Toole EA, Paller AS, Schmuth M, Schwartz J, Sprecher E, Teng JMC, Granier Tournier C, Mazereeuw-Hautier J, Tadini G, Fischer J. Akiyama M, et al. Br J Dermatol. 2025 Sep 18;193(4):619-641. doi: 10.1093/bjd/ljaf154. Br J Dermatol. 2025. PMID: 40308026 Review.
Among the 53 genetically distinct nEDDs are conditions formerly known as autosomal recessive congenital ichthyosis, erythrokeratodermia variabilis et progressiva, Hailey-Hailey disease and Darier-White disease. This review outlines the updated nomenclature an …
Among the 53 genetically distinct nEDDs are conditions formerly known as autosomal recessive congenital ichthyosis, erythrokeratodermia vari …
Dupilumab in the treatment of genodermatosis: A systematic review.
Wu PC, Dai YX, Li CL, Chen CC, Chang YT, Ma SH. Wu PC, et al. J Dtsch Dermatol Ges. 2023 Jan;21(1):7-17. doi: 10.1111/ddg.14924. Epub 2023 Jan 19. J Dtsch Dermatol Ges. 2023. PMID: 36657040
The assessed genodermatoses included Netherton syndrome, epidermolysis bullosa pruriginosa, hyper-IgE syndrome, Hailey-Hailey disease, and severe eczema associated with genetic disorders. Most of the reported cases showed significant clinical improvement afte …
The assessed genodermatoses included Netherton syndrome, epidermolysis bullosa pruriginosa, hyper-IgE syndrome, Hailey-Hailey …
107 results