Results 31 to 40 of about 3,796 (217)

Epilepsie und Morbus Darier - erhöht die Dermatose das Epilepsierisiko? [PDF]

open access: yes, 2019
Morbus Darier ist eine autosomal-dominant vererbte Hautkrankheit aufgrund von Mutationen in dem Gen ATP2A2, das für eine Ca2+-ATPase (SERCA2) kodiert.
Nolting, Julia Kathinka
core   +1 more source

Darier′s disease in gastric malignancy: An unusual paraneoplastic phenomenon

open access: yesIndian Journal of Dermatology, 2015
Darier′s disease is an autosomal dominant genodermatosis resulting from ATP2A2 gene mutation. A 62-year-old male presented at our outpatient (OPD) with sudden-onset numerous dirty, warty papules over the head, neck, and back since 2 months ...
Anusree Gangopadhyay   +5 more
doaj   +1 more source

Exacerbation of Darier Disease under Interferon-α-2a Therapy with Clinical Signs of Lichen Nitidus

open access: yesCase 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

Histology of non-melanoma skin cancers. An Update [PDF]

open access: yes, 2017
Non-melanoma skin cancer (NMSC) is the most frequently diagnosed cancer in humans. Several different non-melanoma skin cancers have been reported in the literature, with several histologic variants that frequently cause important differential diagnoses ...
Cantisani, Carmen   +4 more
core   +2 more sources

A case of zosteriform Darier′s disease with seasonal recurrence

open access: yesIndian 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

Novel mutations in Darier disease and association to self-reported disease severity. [PDF]

open access: yesPLoS 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

Small intestine perforation in a 58-year-old man with Darier disease after 25 months of oral acitretin therapy

open access: yesDermatologica 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

Dowling-Degos Disease: Case Report and Review of the Literature [PDF]

open access: yes, 2010
Dowling-Degos disease (DDD) is an unusual pigmentary disorder usually caused by mutations in keratin 5. A 44-year-old woman in good general health presented due to the recent appearance of numerous pigmented macules on her axillary and anogenital skin. A
Baran, Wojciech   +3 more
core   +1 more source

Darier-White disease [PDF]

open access: yesDermatology 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

Darier White disease

open access: yesNepal 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

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