Results 11 to 20 of about 1,698 (170)
Impaired Calcium Signalling and Neuropsychiatric Disorders in Darier Disease: An Exploratory Review [PDF]
Experimental Dermatology, 2022 Darier (Darier-White) disease (DD) is an autosomal dominant skin disorder caused by pathogenic mutations in the ATP2 A 2 gene which encodes a calcium ATPase in the sarco-endoplasmic reticulum (SERCA2).
Ambur, Austin +3 more
core +4 more sources
An Uncommon Presentation of Darier-White Disease with Hystrix-like Palmoplantar Keratoderma [PDF]
Acta dermatovenerologica Croatica : ADC, 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
core +7 more sources
Darier-White disease of the vulva. Presentation of a patient
Acta Médica del Centro, 2014 The Darier-White disease is an uncommon genodematoses, the transmisision of autosomal dominant, characterized by lesions involving papulokeratosic mucosal and nails; may appear papules on the vulva, specifically.
Mabel González Escudero +2 more
doaj +1 more source
Recurrent corneal ulcerations with perforation in keratosis follicularis (Darier-White disease). [PDF]
Br J Ophthalmol, 2002 Darier-White disease, also known as keratosis follicularis, is a relatively common genodermatosis (frequency between 1 in 36 000 and 1 in 100 000) with autosomal dominant inheritance and late age of onset.1 Clinical features consist of disseminated warty papules and plaques with an affinity to the seborrhoeic areas of the body.
Mielke J, Grüb M, Besch D, Schlote T.
europepmc +3 more sources
Darier disease: Golden era of discovery and global collaborations. [PDF]
J Eur Acad Dermatol VenereolJournal of the European Academy of Dermatology and Venereology, Volume 39, Issue 5, Page 883-884, May 2025.
Labbouz S, Dodiuk-Gad RP.
europepmc +2 more sources
A severe fatal case of Darier-White disease-an extreme phenotype or a new entity? [PDF]
JAAD Case Rep, 2015 Shalom G, Kahn E, Halevy S.
europepmc +2 more sources
Darier disease: Current insights and challenges in pathogenesis and management. [PDF]
J Eur Acad Dermatol VenereolDarier disease (DD) is characterized by the following: Disrupted Ca2+ gradients, impaired desmosomes, impaired keratinocyte differentiation, type 17 inflammation, DC and LC ↓, Th17 cells ↑. DD treatment: First line: keratinocyte focused and/or anti‐inflammatory. Second line: experimental approaches like specific targeting of the inflammatory infiltrate.
Ettinger M +8 more
europepmc +2 more sources
Dermatology Online Journal, 2016 We present a 58-year-old woman with bipolardisorder and with a longstanding history of yellowbrown,hyperkeratotic papules in a seborrheicdistribution and nail changes. Her father andpaternal grandmother had similar eruptions and alsohad psychiatric disease. Histopathologic examinationshowed acantholysis and dyskeratosis, which wasconsistent with Darier-
Christman, Mitalee P +5 more
openaire +4 more sources
Medicina, 2022 Darier disease is an autosomal dominant disorder with dark crusty patches and is classified as hereditary acantholytic dermatosis. Keratotic papules and crust are often present on the scalp, forehead, chest, back, upper arms, elbows, groin, and behind ...
Seok-Young Kang +6 more
doaj +1 more source
Clinical cases of Darier-White follicular dyskeratosis
Medičnì Perspektivi, 2022 Follicular dyskeratosis (Darier-White disease) is a hereditary skin disease that is extremely rare in medical practice, so errors in its diagnosis can occur.
V.Ye. Tkach +5 more
doaj +1 more source