Results 31 to 40 of about 10,294,639 (233)

Naltrexone, a therapeutic alternative in Darier disease

open access: yesRevista Médica del Hospital General de México, 2021
Darier disease is a clinically variable rare disease with autosomal dominant inheritance caused by mutations in ATP2A2 gene. It affects skin, mucous membranes, and nails.
Dennise L. Smith-Pellegrin   +5 more
doaj   +1 more source

Management of Darier disease: A review of the literature and update.

open access: yesIndian Journal of Dermatology, Venereology and Leprology, 2021
Darier disease (DD) is a rare type of inherited keratinizing disorder with no definitive therapeutic approach. The objective of this study is to provide a detailed literature review of all the available treatment modalities of Darier disease, including ...
R. Haber, Nicole Dib
semanticscholar   +1 more source

Vertebral sarcoidosis with associated Darier-Roussy disease manifesting as acute back pain

open access: yesInterdisciplinary Neurosurgery, 2021
Introduction: Sarcoidosis is a systemic granulomatous disease of unknown etiology, with a heterogenous clinical manifestation, progression, and prognosis.
Mohamad Syafeeq Faeez Md Noh   +5 more
doaj   +1 more source

Subcellular compartmentalization of STIM1 for the distinction of Darier disease from Hailey‐Hailey disease

open access: yesJournal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2022
Darier disease (DD) and Hailey‐Hailey disease (HHD) are rare disorders caused by mutations in the ATPase, Sarcoplasmic/Endoplasmic Reticulum Ca2+ Transporting 2 (ATP2A2) and ATPase Ca2+ Transporting Type 2C, Member 1 (ATP2C1) gene, respectively, which ...
H. Stanisz   +5 more
semanticscholar   +1 more source

Darier-White Disease with Sensorineural Hearing Loss – A Case Report

open access: yesRwanda Medical Journal, 2022
Darier-White disease (keratosis follicularis) is a rare autosomal dominant genodermatosis characterized by hyperkeratotic papules and plaques in seborrheic areas, often presenting with nail abnormalities and occasionally mucous membrane changes ...
E. B. Henshaw   +2 more
doaj   +2 more sources

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

Impaired calcium signalling and neuropsychiatric disorders in Darier disease: An exploratory review

open access: yesExperimental Dermatology, 2022
Darier (Darier‐White) disease (DD) is an autosomal dominant skin disorder caused by pathogenic mutations in the ATP2A2 gene which encodes a calcium ATPase in the sarco‐endoplasmic reticulum (SERCA2). Defects in the SERCA2 protein lead to an impairment of
Austin B. Ambur   +3 more
semanticscholar   +1 more source

Darier disease, hypertrophic / vegetating type

open access: yesSurgical and Experimental Pathology, 2022
Background A hypertrophic / vegetating variant of Darier disease causing massive verruciform genital tumors is exceedingly rare. Case presentation A woman in her late 50s underwent wide resection of vulva and inguinal skin due to massive verruciform ...
Caroline Passos Cardoso   +4 more
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′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

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