Results 21 to 30 of about 1,856 (171)
Exacerbation of Darier Disease under Interferon-α-2a Therapy with Clinical Signs of Lichen Nitidus
Case Reports in Dermatology, 2016 Darier disease/dyskeratosis follicularis is a genodermatosis characterized by brown, oily keratotic papules and plaques in the seborrheic areas of the face and chest.
Ioannis Karagiannidis +2 more
doaj +1 more source
Novel mutations in Darier disease and association to self-reported disease severity. [PDF]
PLoS ONE, 2017 Darier disease is a rare and severe autosomal dominant skin disease characterised by malodorous keratotic papules in seborrheic areas of the skin. Darier disease affects up to 1 in 30 000 people and is caused by mutations in the ATP2A2 gene, which ...
Ivone U S Leong +4 more
doaj +1 more source
Dermatologica Sinica, 2014 Darier disease is a rare autosomal dominant disease characterized by abnormal keratinization of the epidermis, mucosa, and nails. Acitretin, an aromatic form of tretinoin, is widely prescribed in the treatment of Darier disease.
Yi-Hao Wang, Dino Tsai
doaj +1 more source
Nepal Journal of Dermatology, Venereology & Leprology, 2012 Darier’s disease was described inependently by Darier and White in 1989 AD. Reported prevalence varies from 1/100,000 in Denmark to 1 in 30- 35,000 in northern England and Scotland.1 Darier’s disease has been reported from other parts of the world ...
A Amatya +5 more
doaj +3 more sources
A case of zosteriform Darier′s disease with seasonal recurrence
Indian Dermatology Online Journal, 2013 Darier′s disease is an uncommon genodermatosis characterized by keratotic papules in seborrheic distribution. The disease can rarely present in unilateral zosteriform pattern, as a mosaic form following the Blaschko′s line. We present a 35-year-old woman
Lalit K Gupta +3 more
doaj +1 more source
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
Indian Journal of Paediatric Dermatology, 2023 Darier disease (DD) and acrokeratosis verruciformis of Hopf are rare autosomal dominant skin disorders. Both are caused by a single gene mutation, i.e., ATP2A2 located on chromosome 12, which is expressed in the skin and brain. However, both the diseases
Avinash Sharma +3 more
doaj +1 more source
Darier-White disease in siblings responding to isotretinoin
Indian Dermatology Online Journal, 2010 Darier-White disease (keratosis follicularis) is a rare disorder of keratinization involving the epidermis, mucous membranes, and nails. It is said to occur as a result of mutation in the ATP2A2 gene located on chromosome 12q23-24.1.
Ramesh M Bhat +3 more
doaj +1 more source
Grover's disease: dermoscopy, reflectance confocal microscopy, and histopathological correlation
Dermatology Practical & Conceptual, 2017 Grover’s disease is a benign condition of unknown origin characterized clinically by an erythematous papulovesicular eruption and histopathologically by intraepidermal clefting and four different patterns of acantholysis: Darier-like, pemphigus-like ...
Francesco Lacarrubba +4 more
doaj +1 more source
Darier-White disease and Psychiatric disorders: A Case Report
European Psychiatry, 2022 Introduction Darier-White disease (DD) is a rare genodermatosis of dominant autosomic inheritance characterized by the keratinization of epidermis, nails and mucous membrane.
R.L. Esteve +3 more
doaj +1 more source