Darier disease: a case report

Darier disease, also known as keratosis follicularis, dyskeratosis follicularis, and benign dyskeratosis, is a rare disorder of keratinisation that primarily affects the skin and, to a lesser extent, the oral mucosa. It was described independently by both Darier and White in 1889. It has a prevalenc...

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Main Authors: Jalil, A.A., Zain, R.B., van der Waal, I.
Format: Article
Language:English
English
Published: Elsevier 2005
Subjects:
Online Access:http://eprints.um.edu.my/2431/2/Darier.pdf
http://eprints.um.edu.my/2431/1/Darier_disease_A_case_report.pdf
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author Jalil, A.A.
Zain, R.B.
van der Waal, I.
author_facet Jalil, A.A.
Zain, R.B.
van der Waal, I.
author_sort Jalil, A.A.
collection UM
description Darier disease, also known as keratosis follicularis, dyskeratosis follicularis, and benign dyskeratosis, is a rare disorder of keratinisation that primarily affects the skin and, to a lesser extent, the oral mucosa. It was described independently by both Darier and White in 1889. It has a prevalence of 1:100,000 of the population and is inherited as an autosomal dominant trait.1 The age of onset is childhood or adolescence. Patients usually present with multiple small firm reddish-brown papules on the forehead, scalp, neck, shoulders, chest, and limbs. Other cutaneous signs include punctate keratotic pits of the palms and soles and dystrophy of the nails, which is characterised by a red and white sandwich of streaks associated with a V-shaped notch. The oral lesions are usually asymptomatic and are seen as multiple, normal-coloured or white flat-topped papules that predominantly affect the palate.
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spelling um.eprints-24312014-10-20T05:25:55Z http://eprints.um.edu.my/2431/ Darier disease: a case report Jalil, A.A. Zain, R.B. van der Waal, I. R Medicine RK Dentistry Oral surgery Darier disease, also known as keratosis follicularis, dyskeratosis follicularis, and benign dyskeratosis, is a rare disorder of keratinisation that primarily affects the skin and, to a lesser extent, the oral mucosa. It was described independently by both Darier and White in 1889. It has a prevalence of 1:100,000 of the population and is inherited as an autosomal dominant trait.1 The age of onset is childhood or adolescence. Patients usually present with multiple small firm reddish-brown papules on the forehead, scalp, neck, shoulders, chest, and limbs. Other cutaneous signs include punctate keratotic pits of the palms and soles and dystrophy of the nails, which is characterised by a red and white sandwich of streaks associated with a V-shaped notch. The oral lesions are usually asymptomatic and are seen as multiple, normal-coloured or white flat-topped papules that predominantly affect the palate. Elsevier 2005 Article PeerReviewed application/pdf en http://eprints.um.edu.my/2431/2/Darier.pdf application/pdf en http://eprints.um.edu.my/2431/1/Darier_disease_A_case_report.pdf Jalil, A.A. and Zain, R.B. and van der Waal, I. (2005) Darier disease: a case report. British Journal of Oral and Maxillofacial Surgery, 43 (4). pp. 336-338. ISSN 0266-4356, DOI https://doi.org/10.1016/j.bjoms.2004.10.017 <https://doi.org/10.1016/j.bjoms.2004.10.017>. 10.1016/j.bjoms.2004.10.017
spellingShingle R Medicine
RK Dentistry
Oral surgery
Jalil, A.A.
Zain, R.B.
van der Waal, I.
Darier disease: a case report
title Darier disease: a case report
title_full Darier disease: a case report
title_fullStr Darier disease: a case report
title_full_unstemmed Darier disease: a case report
title_short Darier disease: a case report
title_sort darier disease a case report
topic R Medicine
RK Dentistry
Oral surgery
url http://eprints.um.edu.my/2431/2/Darier.pdf
http://eprints.um.edu.my/2431/1/Darier_disease_A_case_report.pdf
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