Clinicopathologic findings of guttate leukoderma in Darier disease: A helpful diagnostic feature
JAAD Case Reports, 2018 DD: Darier disease GL: guttate leukoderma IGH: idiopathic guttate hypomelanosis INTRODUCTION Darier disease (DD), also known as keratosis follicularis or Darier-White disease, is a rare autosomal dominant genodermatosis attributed to a mutation in the ...
J. Harb, K. Motaparthi
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An Uncommon Presentation of Darier-White Disease with Hystrix-like Palmoplantar Keratoderma [PDF]
, 2021 Darier-White disease is a relatively common autosomal dominant genodermatosis caused by mutation in the ATP2A2 gene. It is characterized by multiple warty papules coalescing into plaques in the seborrheic areas and by specific histological skin changes ...
Ellenbogen, Eran +6 more
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Combination of alitretinoin and topical 5-fluorouracil in Darier disease
JAAD Case Reports, 2018 DD: Darier disease 5-FU: 5-fluorouracil INTRODUCTION Darier disease (DD) is a rare autosomal dominant genodermatosis that is clinically characterized by papular keratotic lesions predominant in seborrheic areas (chest, back, armpits). Bacterial and viral
A. Soenen +5 more
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Drug-related pityriasis rubra pilaris with acantholysis [PDF]
, 2013 Introduction. Acantholysis is rarely reported histological feature of Pityriasis rubra pilaris (PRP), recently recognized as having diagnostic specificity for differentiating PRP from psoriasis. Case report.
Duran Verica D. +5 more
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Acral Hemorrhagic Darier Disease.
Actas Dermo-Sifiliográficas, 2017 Darier disease is an autosomal-dominant inherited condition caused by mutation of a gene, which produces a protein involved in calcium channel regulation.
M. Flores-Terry +4 more
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Subcutaneous Sarcoidosis. A Rare Case of Specific Cutaneous Involvement [PDF]
, 2012 A sarcoidose é uma doença granulomatosa multissistémica de etiologia desconhecida. O envolvimento cutâneo pode ocorrer, sendo classificado de específico ou inespecífico, dependendo da presença ou ausência de granulomas no exame histopatológico da pele ...
Afonso, A +3 more
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Journal of Nippon Medical School = Nippon Ika Daigaku zasshi, 2017 Darier disease (DD) is a rare autosomal dominant skin disorder due to mutations in the ATP2A2 gene, which encodes sarco/endoplasmic reticulum Ca2+ ATPase isoform 2 (SERCA2). The clinical manifestations of DD are characterized by warty papules and plaques
Min Li, N. Higashi, H. Nakano, H. Saeki
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Darier disease with oral and esophageal involvement: A case report
Indian Journal of Dental Research, 2011 A 58-year-old man presented with itchy papular eruptions all over the body since 15 years. Intraoral examination revealed raised papular lesions on the labial mucosa, hard palate, and tongue.
Magesh Karuppur Thiagarajan +2 more
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A plazmamembrán Ca2+ ATPáz 4b izoforma apoptotikus fragmentjét reprezentáló mutáns sejten belüli lokalizációja, stabilitása, hatásai a sejtek Ca2+ háztartására és szerepe az apoptózis folyamatban = Intracellular localization and stability of a mutant representing the apoptotic fragment of the plasma membrane Ca2+ ATPase 4b and its role in cellular Ca2+ homeostasis and apoptosis [PDF]
, 2010 A jelen kutatási periódus alatt egy fontos Ca2+ transzport fehérje, a plazma membrán Ca2+ ATPáz (PMCA4b) struktúra/funkció változásait tanulmányoztuk az apoptózis valamint a nekrózis folyamatai alatt. Eredményeink azt bizonyítják, hogy a PMCA4b fehérjét -
Antalffy, Géza +5 more
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Haemorrhagic Darier's Disease [PDF]
Journal of the Royal Society of Medicine, 1989 I H, Coulson, K J, Misch
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