Literature DB >> 1619075

Darier-White disease: a review of the clinical features in 163 patients.

S M Burge1, J D Wilkinson.   

Abstract

BACKGROUND: Darier's disease is a rare, dominantly inherited genodermatosis; there have not been any large clinical studies of patients with this disease.
OBJECTIVE: Our purpose was to document the clinical features in a large group of patients with Darier's disease.
METHODS: Data were collected from 163 affected persons.
RESULTS: The onset usually occurred between the ages of 6 and 20 years. The disease has a predilection for the skin in seborrheic areas; 96% had acral signs; 6% had hypertrophic flexural involvement; and 13% had oral mucosal lesions. There was no remission. Topical therapy sometimes provided relief of symptoms but had no effect on the progress of the disease. Oral retinoids were effective, but long-term therapy was tolerated poorly. Most patients did not have other medical problems.
CONCLUSION: Although Darier's disease is a chronic and unremitting burden, most patients manage to lead a relatively normal life.

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Year:  1992        PMID: 1619075     DOI: 10.1016/0190-9622(92)70154-8

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  47 in total

1.  Recurrent corneal ulcerations with perforation in keratosis follicularis (Darier-White disease).

Authors:  J Mielke; M Grüb; D Besch; T Schlote
Journal:  Br J Ophthalmol       Date:  2002-10       Impact factor: 4.638

Review 2.  [Possible genetic link between Darier's disease and depression. Review of the literature and case history].

Authors:  D R Bach; F Moggi; T J Müller; E Seifritz; W K Strik; G Wirtz
Journal:  Nervenarzt       Date:  2007-01       Impact factor: 1.214

Review 3.  Darier's disease: a calcium-signaling perspective.

Authors:  B Pani; B B Singh
Journal:  Cell Mol Life Sci       Date:  2008-01       Impact factor: 9.261

4.  [Segmental Darier disease : treatment with pulsed dye laser].

Authors:  L Schmitt; S Roos; C Raulin; S Karsai
Journal:  Hautarzt       Date:  2009-12       Impact factor: 0.751

5.  Genetic linkage for Darier disease (keratosis follicularis).

Authors:  J L Kennedy; D Berg; A S Bassett; R Roy; N King; M Perkins
Journal:  Am J Med Genet       Date:  1995-01-30

Review 6.  Endoplasmic-reticulum calcium depletion and disease.

Authors:  Djalila Mekahli; Geert Bultynck; Jan B Parys; Humbert De Smedt; Ludwig Missiaen
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-06-01       Impact factor: 10.005

7.  Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region.

Authors:  S Monk; A Sakuntabhai; S A Carter; S D Bryce; R Cox; L Harrington; E Levy; V L Ruiz-Perez; E Katsantoni; A Kodvawala; C S Munro; S Burge; M Larrègue; G Nagy; J L Rees; M Lathrop; A P Monaco; T Strachan; A Hovnanian
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

8.  Linkage analysis between schizophrenia and the Darier's disease region on 12q.

Authors:  M P O'Malley; A S Bassett; W G Honer; J L Kennedy; N King; D Berg
Journal:  Psychiatr Genet       Date:  1996       Impact factor: 2.458

9.  [46/f with itchy skin lesions in seborrheic areas : Preparation for the specialist examination: part 7].

Authors:  D Boehmer; K Eyerich
Journal:  Hautarzt       Date:  2018-11       Impact factor: 0.751

10.  Recurrent presumed herpes simplex keratitis and episcleritis in keratosis follicularis (Darier's disease).

Authors:  Meera Radia; Michael James Gilhooley; Chris Panos; Charles Claoué
Journal:  BMJ Case Rep       Date:  2015-07-16
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