Karger Publishers Effectiveness of Topical Adapalene in Dowlingdegos disease The clinicalaspect of Dowling-degos disease (DDD) is clearly summarized in the descriptive http://content.karger.com/ProdukteDB/produkte.asp?Doi=18102
AFRH, Maladie De Verneuil, Hidrosadenite Suppuree Reticulated pigmented anomaly of the flexures (Dowlingdegos disease) is a We report a case of Dowling-degos disease in association with acne inversa. http://www.afrh.fr/Dowling-Degos.html
Extractions: Hautarzt 2001 Jul;52(7):642-645 [ article en allemand ] Kleeman D, Trueb RM, Schmid-Grendelmeier P. Dermatologische Klinik, Universitatsspital Zurich, Gloriastrasse 31, Ch-8091 Zurich. Reticulated pigmented anomaly of the flexures (Dowling-Degos disease) is a rare autosomal-dominant genodermatosis with variable penetrance that is characterized by reticulated hyperpigmentation of the flexures. Acne inversa has been previously described in the literature under several synonyms, such as acne triad, acne tetrad and hidradenitis suppurativa. Acne inversa is an inflammation affecting the pilosebaceous units of the flexures. We report a case of Dowling-Degos disease in association with acne inversa. The association of these diseases has been described several times and it appears not to be coincidental. Pathogenetic mechanisms leading to this coincidence are discussed. Clin Exp Dermatol 1996 Jul;21(4):305-6 Dowling-Degos disease associated with hidradenitis suppurativa. A case of Dowling-Degos disease coexisting with hidradenitis suppurativa is described. We propose that the follicular occlusion inherent in Dowling-Degos disease may predispose to the development of hidradenitis suppurativa. Cutis Jun;45(6):446-50 1990
A.F.R.H., Maladie De Verneuil; Hidrosadénite Suppurée Hidradenitis suppurativa, Dowling degos disease and perianal squamous cell carcinoma.Li M, Hunt MJ, Commens CA. Department of Dermatology, Westmead http://www.afrh.fr/1997.html
Extractions: "Tous ensemble pour la Recherche de traitements et de solutions" Accueil Livre d'or Forum T'chat ... Contact A.F.R.H. Qui sommes-nous? Statuts -Actions Publications Plaquette ... Dossier de Presse Patients Qui touche-t-elle ? Traitements Trucs et Astuces Galerie photos ... Groupe de soutien Soutien Don Cartes Piano-Bar Peluches Australas J Dermatol 1997 Nov;38(4):209-11 Hidradenitis suppurativa, Dowling Degos disease and perianal squamous cell carcinoma. Li M, Hunt MJ, Commens CA Department of Dermatology, Westmead Hospital, Sydney, New South Wales, Australia. A patient with hidradenitis suppurativa (HS) is described in association with Dowling Degos disease and perianal squamous cell carcinomas. As the initial treatment for HS failed to give any satisfactory relief he sought no further medical help for the subsequent 40 years. This patient illustrates the management difficulties in HS and the need for regular surveillance to exclude the development of anogenital squamous cell carcinoma. Previous reports of hidradenitis suppurativa in association with Dowling Degos disease are reviewed and the aetiology is discussed.
Blackwell Synergy - Cookie Absent On the basis of these findings the diagnosis of degos disease was suspected. In most cases of classical degos disease the diagnosis was established post http://www.blackwell-synergy.com/doi/abs/10.1111/j.1468-3083.2004.01181.x
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Blackwell Synergy - Cookie Absent Histology confirmed the clinical diagnosis of degos disease. degos disease is arare disorder that has been classified into the benign or malignant variety. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1365-4632.2004.02080.x
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Portal Toolkit Invalid Site URL Some cases of Dowlingdegos disease have associated reticulate pigmentation of The mutation locus in Dowling-degos disease is still to be determined. http://ppv.ovid.com/pt/re/aujd/fulltext.00000936-200108000-00015.htm
Portal Toolkit Invalid Site URL Degos disease radiological and immunological aspects The etiology of thevasculitis in degos disease remains unknown, despite the number of reported http://ppv.ovid.com/pt/re/obes/fulltext.00000132-199611000-00010.htm
Degos' Disease - General Practice Notebook degos disease 1 tray.dermatology.uiowa . Image DermIS main menu DOIA DowlingDegos Diseas www.dermis.net/doia/ima Image 2 Genodermatoses http://www.gpnotebook.co.uk/medwebpage.cfm?ID=53805076
Paul Arky Design [Paul Arkinstall] / Portfolio / Websites This is a websitededicated to helping patients, their families, carers and friends to understanddegos disease. Website www.degosdisease.com. http://www.paularky.co.uk/portfolio/websites/degosdisease.htm
1st International Meeting On Degos Disease 1st International Meeting on degos disease. dermatology, pathology, neurology,diseases of the gastrointestinal tract, degos disease, DD, http://mediconf.de/recstitl/23000104.HTM
Extractions: MediConf World Calendar of Medical Events 1st International Meeting on Degos Disease dermatology, pathology, neurology, diseases of the gastrointestinal tract, Degos disease, DD, malignant atrophic papulosis, papulosis atrophicans maligna, Kohlmeier-Degos-Delort-Tricot syndrome, lethal cutaneous and gastrointestinal arteriolar thrombosis For details on this meeting and more meetings in the same field visit our Medical Specialty Calendar MediConf lists over 10000 future events including conferences, workshops, seminars, symposia and exhibitions in the fields of medicine, healthcare, pharmacology, and biotechnology. Every medical specialty is included, from allergy to zoonoses. MediConf is an excellent source of information for healthcare professionals and the pharmaceutical industry worldwide.
AJNR -- Sign In Page degos disease (also known as malignant atrophic papulosis or KohlmeierDegos The neurologic manifestations of degos disease include cerebral infarcts, http://www.ajnr.org/cgi/content/full/26/3/646
Extractions: This Article Abstract Figures Only Full Text (PDF) ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Amato, C. Articles by Moschini, M. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 7 days for US$10.00 Pay for Admission - You may access all content in American Journal of Neuroradiology Online (from the computer you are currently using) for 7 days for US$25.00.
Extractions: This Article Figures Only Full Text Full Text (PDF) ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Amato, C. Articles by Moschini, M. American Journal of Neuroradiology 26:646-649, March 2005
ThirdAid.com - The World S First Dedicated Online Patient To (Kohlmeierdegos disease , Degos-Kohlmeier Disease , Degos Syndrome , MalignantAtrophic Papulosis ). degos disease. (Kohlmeier-degos disease http://www.thirdaid.com/index/qfm/fuseaction/registrationStep3/letter/D
Vasculitis degos disease. This is the Web site of the Degos Patients Support Network.degos disease is a rare disease, also known as malignant atrophic papulosis, http://omni.ac.uk/browse/mesh/D014657.html
Extractions: low graphics broader: Vascular Diseases other: Aneurysm Angioneurotic Edema Arteriovenous Malformations Cerebrovascular Disorders ... Varicose Veins narrower: Behcet Syndrome Mucocutaneous Lymph Node Syndrome Thromboangiitis Obliterans Vasculitis This interactive tutorial on vasculitis, a group of diseases that causes blood vessels to become inflamed, has been produced by the Patient Education Institute, and made available on the Web by the National Library of Medicine MEDLINEplus service. The tutorial provides background information on vasculitis and covers causes, clinical signs and symptoms, diagnosis, and treatment. Viewing this tutorial requires Flash plug-in. Vasculitis Teaching Materials Patient Education Degos disease This is the Web site of the Degos Patients Support Network. Degos Disease is a rare disease, also known as malignant atrophic papulosis, initially presenting as a skin condition characterised by red papules with white centres, and telangiectasia. Serious (possibly fatal) gastrointestinal and neurologic symptoms usually follow. This Web site brings together what little is know about the condition, providing information for patients and clinicians on symptoms, diagnosis treatment and prognosis. Vasculitis Thromboangiitis Obliterans
Extractions: Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Dastur, D. K. Articles by Shroff, H. J. Journal of Neurology, Neurosurgery, and Psychiatry, 1981, Vol 44, 156-160 DK Dastur, BS Singhal and HJ Shroff
Papulosis, Malignant Atrophic degos disease was named after Dr Degos who recognized this disease as a distinctentity in 1942 degos disease, also called malignant atrophic papulosis, http://www.orpha.net/static/GB/papulosis.html
Extractions: Submit a response Alert me when this article is cited Alert me when Correspondence are posted ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Horner, F. A. Articles by Choi, B. H. FA Horner, GJ Myers, DA Stumpf, BJ Oseroff and BH Choi Malignant atrophic papulosis (Kohlmeier-Degos disease) is reported for the first time with pathologic verification of central nervous system involvement in a child. The disease began in infancy with rare recurring skin lesions; the child died at the age of 7, after progressive neurologic deterioration. Diagnosis was suspected clinically and confirmed by biopsy of a typical skin lesion. Recognition of this disorder by its dermatologic
