61. Mayo Clinic Proceedings Katz SK, Mudd LJ, Roenigk HH Jr. malignant atrophic papulosis (Degos’ disease)involving three generations of a family. J Am Acad Dermatol. http://www.mayoclinicproceedings.com/inside.asp?AID=17&UID=

62. Disease, Medication, Symptom Etc Database Index : M Diseases Database malignant atrophic papulosis see Degos disease Malignant fibrous histiocytoma Malignant hepatopathy Malignant hyperpyrexia Malignant hypertension http://www.diseasesdatabase.com/disease_index_m.asp

Diseases Database Index Sponsors Contact ... Previous Page Disease, medication, symptom etc database index : M Search Machado-Joseph Azorean disease Machupo virus see Bolivian hemorrhagic fever MacLeod syndrome Macroamylasaemia Macroamylase see Macroamylasaemia Macrocephaly see Megencephaly Macrocornea see Megalocornea Macrocytic red blood cell see Macrocytosis (erythrocyte) Macrocytosis (erythrocyte) Macroglossia Macrogyria see Pachygyria Macrolactams Macrolides Macromastia see Breast hypertrophy Macroorchidism see Testicular enlargement Macro-orchidism see Testicular enlargement Macrophage migration inhibitory factor Macrosomia Macrostomia ... Macrothrombocytosis Macular atrophy, Jadassohn type see Anetoderma Macular atrophy, Schweninger-Buzzi type see Anetoderma Macular hole Macular pucker see Epiretinal membrane Macular star see Hard retinal exudate Maculopapular rash Maculopathy Maculopathy, age related see Senile macular retinal degeneration Madelung deformity Madelung-Launois-Bensaude syndrome see Benign symmetrical lipomatosis of Madelung Madura foot see Mycetoma Madurella mycetomi Maduromycosis see Mycetoma Mafenide Maffucci syndrome see Enchondromatosis Maggot infestation see Myiasis Magnesium chloride Magnesium hydroxide Magnesium levels low (plasma or serum) see Hypomagnesemia Magnesium levels raised (plasma or serum) see Hypermagnesaemia Magnesium oxide Magnesium salts Magnesium sulfate Magnesium sulphate see Magnesium sulfate Mahaim-type preexcitation Maidenhair tree see Gingko biloba Mairungi see Khat Majewski syndrome see Short rib-polydactyly syndrome type 2 Majocchi granuloma

63. Degos' Disease Information Diseases Database malignant atrophic papulosis. may cause or feature + (Follow link for list.)belong(s) to the category of + (Follow link for list.) No UMLS definitions.. http://www.diseasesdatabase.com/ddb29425.htm

Diseases Database Index Sponsors Contact ... Previous Page Degos' disease information Search 4 synonyms or equivalents were found. Degos' disease aka/or Erythrokeratoderma en cocardes aka/or Kohlmeier-Degos disease aka/or Malignant atrophic papulosis may cause or feature (Follow link for list.) belong(s) to the category of (Follow link for list.) No UMLS definitions. Degos' disease: specific web sites Send Degos' disease to medical search engines (JavaScript enabled browsers only.) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation Valid XHTML 1.0 Served 2005-09-09 11:10:09 View metadata Last major update 2005-09-03. The medical information here is presented for education, background reading and general interest. The Diseases Database is not a diagnostic or clinical decision-making tool. Please consult your own licensed physician regarding diagnosis and treatment of any medical condition! Content is not asserted complete or error free, please see also our

64. Definitions Of Genetic Disorders-M. Malignant Astrocytoma astromal.htm malignant atrophic papulosis degos.htm MalignantFever mh.htm Malignant Hyperphenylalaninemia atyphyp.htm http://www.icomm.ca/geneinfo/def-m.htm

65. American Family Physician: Dermatomyositis malignant atrophic papulosis (Degos disease). Zebralike striping. Vulvar/scrotalinvolvement. Heliotrope, a macular rash with periorbital edema, http://www.findarticles.com/p/articles/mi_m3225/is_9_64/ai_80099707

@import url(/css/us/style1.css); @import url(/css/us/searchResult1.css); @import url(/css/us/articles.css); @import url(/css/us/artHome1.css); Advanced Search Home Help IN free articles only all articles this publication Automotive Sports 10,000,000 articles - not found on any other search engine. FindArticles American Family Physician Nov 1, 2001 Content provided in partnership with 10,000,000 articles Not found on any other search engine. Featured Titles for AAACN Viewpoint ABNF Journal, The AIDS Treatment News AMAA Journal ... View all titles in this topic Hot New Articles by Topic Automotive Sports Top Articles Ever by Topic Automotive Sports Dermatomyositis American Family Physician Nov 1, 2001 by Ric Anthony Koler Andrew Montemarano Save a personal copy of this article and quickly find it again with Furl.net. It's free! Save it. Dermatomyositis is an idiopathic inflammatory myopathy with characteristic skin manifestations. Although the disorder is rare, with a prevalence of one to 10 cases per million in adults and one to 3.2 cases per million in children, early recognition and treatment are important ways to decrease the morbidity of systemic complications. An association with other connective tissue disorders (overlap syndrome) and malignancy make this diagnosis particularly important to primary care physicians. Patient management includes careful evaluation for underlying malignancy and liberal use of physical therapy, antihistamines, sunscreen and oral corticosteroids. Poor prognostic indicators include poorly responsive disease, delay in diagnosis and the presence of malignancy. The therapeutic goal is to maintain function and prevent or minimize sequelae. (Am Fam Physician 2001;64:1565-72.)

66. Degos Disease Degos disease, also known as malignant atrophic papulosis is a rare disorder.It affects the lining of the small blood vessels resulting in blockage. http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Degos_disease?Ope

67. Index M: Contact A Family - For Families With Disabled Children: Information On malignant atrophic papulosis see Degos disease Malignant Hyperpyrexia see MalignantHyperthermia Malignant Hyperthermia Mandibulo Dysostosis see Treacher http://www.cafamily.org.uk/Idx/m.html

printer friendly home how we can help medical information ... how you can help Please use the index below to access the condition you require information on. It may take longer to find what you are looking for this way compared with our "search this site" facility in the navigator on the left but we try to point you in the most appropriate direction using this index and therefore the results should be better. For speed, this index has been split into separate alphabetical files: numbers 0-9 A B C ... Z Contact a Family also has information on many other specific conditions and rare disorders. If you cannot find the information you require in The Contact a Family Directory Online , you may wish to use our Contact a Family Helpline service. MAD see Fatty Acid Oxidation Disorders MCAD see Fatty Acid Oxidation Disorders M-CMTC syndrome MDA see MDC1A see Congenital Muscular Dystrophy MDC1C see Congenital Muscular Dystrophy MDS see Lissencephaly ME see Chronic Fatigue syndrome / Myalgic Encephalopathy MEB see Congenital Muscular Dystrophy and Lissencephaly MED see Perthes disease MELAS see Metabolic diseases and see Mitochondrial Cytopathies and related disorders MEN I see Multiple Endocrine Neoplasia Type I MEN II see Multiple Endocrine Neoplasia Type II MEN IIA see Multiple Endocrine Neoplasia Type II MEN IIB see Multiple Endocrine Neoplasia Type I I MERRF see

68. DEGOS DISEASE: Contact A Family - For Families With Disabled Children: Informat Degos disease malignant atrophic papulosis KohlmeierDegos disease. Degos diseaseis a rare inherited condition first described by Kohlmeier in 1941 and http://www.cafamily.org.uk/Direct/d19.html

printer friendly DEGOS DISEASE home how we can help medical information index of conditions ... how you can help Did you find this page helpful? yes no Degos disease: Malignant Atrophic Papulosis: Kohlmeier-Degos disease Degos disease is a rare inherited condition first described by Kohlmeier in 1941 and Degos in 1942. There are thought to have been about 150 cases of the condition reported in medical literature. The most severe form is Systemic Degos disease affecting children and adolescents with most cases occurring in young adults. Benign Degos disease also affects adults. Systemic Degos disease affects a number of body systems: Skin - pink or red papules (solid raised lesions) primarily on the trunk and limbs healing to leave white scars; Gastrointestinal - abdominal pain, nausea, vomiting, diarrhoea or constipation and, in the later stages, intestinal perforation and haemorrhage may occur; Neurological - manifestations involve the peripheral and central nervous systems leading to headaches, dizziness, seizures, hemiplegia (total or partial paralysis of one side of the body), aphasia (loss or impairment of the power to use or comprehend words), paraplegia (paralysis of the lower half of the body), and gaze palsy (partial or complete inability to move the eyes to all directions of gaze); Ocular - ptosis (drooping of the upper eyelid), optic neuritis (inflammation of optic nerves), diplopia (double vision) and visual field defects may occur.

69. UWCM Department Of Dermatology malignant atrophic papulosis (Degos disease) clinicopathological correlations.JEADV 2001; 15 4345. Chowdhury MMU, Chakrabarti A, Prais L, http://www.dermatology.org.uk/portal/asp/pubs0102.html

Department of Dermatology Publications 2001-2002 Listed Alphabetically Research Papers Anstey AV. Photomedicine: Lessons from the Smith-Lemli-Opitz syndrome. J Photochemistry Photobiology 2001; 62: 123-7 Azurdia RM, Anstey AV, Rhodes LE. High cholesterol diet improves the photosensitivity in Smith-Lemli-Opitz syndrome. Br J Dermatol 2001; 144: 143-5 Chave T A, Varma S, Patel G K, Knight A G .Malignant atrophic papulosis (Degos' disease): clinicopathological correlations. JEADV 2001; 15: 43-45. Chowdhury M M U, Chakrabarti A, Prais L, Foulds I S. Occupational allergic contact dermatitis caused by 5,7-dichloro-4(4-fluorophenoxy) quinolone (quinoxyfen). Contact Dermatitis 2001; 45: 119-20. Chowdhury M M U, Motley R J. Treatment of acrodermatitis continua of Hallopeau with oral propylthiouracil and methotrexate. Clin Exp Dermatol 2001; 26: 657-60. Chowdhury M M U, Statham B N. Allergic contact dermatitis from dibutyl phthalate and benzalkonium chloride in Timodine®. Contact Dermatitis 2002; 46: 57. Chowdhury M M U, Inaloz H S, Motley R J, Knight A G. Erythema elevatum diutinum and IgA paraproteinaemia: 'a preclinical iceberg'. Int J Dermatol 2002; 41: 368-70.

70. UWCM Department Of Dermatology Publications malignant atrophic papulosis (Degos disease) clinicopathological correlations.J Eur Acad Dermatol Venereol 2001; 15 4345. CHOWDHURY MMU. http://www.dermatology.org.uk/portal/asp/pubs0001.html

Department of Dermatology Publications 2000-2001 Listed Alphabetically Research Papers ANSTEY AV. Drug reactions and the skin. Medicine 2000; 28: 12: 63-64. CHAVE TA, CHOWDHURY MMU, HOLT PJA. Recalcitrant necrobiotic xanthogranuloma responsive to pulsed oral dexamethasone and maintenance prednisolone. Br J Dermatol 2001; 144: 158-61. CHAVE TA, FINLAY AY, KNIGHT AG - On behalf of the All Wales Dermatology Audit Committee. Thalidomide usage in Wales: the need to follow guidelines. Br J Dermatol 2001; 144: 310-315. CHAVE T, VARMA S, LOGAN R, HOLT PJA. A papillary lesion on the foreskin. Arch Dermatol 2001; 137: 815-20 (off-centre). CHAVE TA, VARMA S, PATEL GK, KNIGHT AG. Malignant atrophic papulosis (Degos' disease): clinicopathological correlations. J Eur Acad Dermatol Venereol 2001; 15: 43-45. CHOWDHURY MMU. The management of psoriasis in primary care. Prescriber 2000; 11(18): 99-107. CHOWDHURY MMU, ANSTEY AV. Dermatological Pharmacology. Medicine 2000; 28(11): 12-16. CHOWDHURY MMU, ANSTEY A, MATTHEWS CAN. The dermatosis of chronic granulomatous disease. Clin Exp Dermatol: 2000; 25:190-4.

71. Portal Toolkit Invalid Site URL CNS involvement in malignant atrophic papulosis (KohlmeierDegos disease)vasculopathy and coagulopathy. J Neurol Neurosurg Psychiatry 1981 44 156-160. http://ppv.ovid.com/pt/re/obes/fulltext.00000132-199611000-00010.htm

Sorry, the URL specified, http://ppv.ovid.com:80/pt/re/obes/fulltext.00000132-199611000-00010.htm , is invalid. To go to site for "OvidPPV" please click here http://ppv.ovid.com To go to site for "Acta Neurologica Scandinavica" please click here http://www.lwwonline.com To go to the LWW Online site, please click here http://www.lwwonline.com Thank you

72. All Topics - Quest Diagnostics Patient Health Library Degos Disease (malignant atrophic papulosis) Support Group. Degos PatientsSupport Network Degos Disease (malignant atrophic papulosis) Support Group http://www.questdiagnostics.com/kbase/list/all/d.htm

All Topics Click a letter to see a list of topics beginning with that letter. A B C E ... D-Xylose Absorption Test [Medical Test] DA Da Costa's Syndrome Dacryosialoadenopathia Dacryosialoadenopathy DAD-to-DAD - Parenting / Grandparenting [Support Group] Dalpro, Fetal Effects From Dana Farber Cancer Institute Family Studies Cancer Risk Line - Cancer Helpline [Support Group] Danazol [Medication] Danazol for endometriosis [Medication] Danazol for severe PMS (premenstrual dysphoric disorder) [Medication] Danbolt-Cross Syndrome Dancing Eye Syndrome [Support Group] Dancing Eye Syndrome - Dancing Eye Syndrome [Support Group] Dandruff Dandruff Dandy Fever Dandy Walker Malformation ... Dandy Walker Syndrome [Support Group] Dandy-Walker Cyst Dandy-Walker Deformity Dandy-Walker Syndrome Dandy-Walker Syndrome Network - Dandy Walker Syndrome [Support Group] Danish Cardiac Type Amyloidosis (Type III) Darier Disease Darier-White Disease Top Davidson's Disease Davies' Disease Dawson's Disease Dawson's Encephalitis ... Daycare DB DB-Link (National Information Clearinghouseon Children who are Deaf/Blind) - Blind Helpline [Support Group] DBA DBS DD DD DE De Barsy Syndrome De Barsy-Moens-Diercks Syndrome de Lange Syndrome De Morsier Syndrome ... Deaf / Hearing Impaired / Tinnitus / Meniere's [Support Group] Deaf Helpline [Support Group] Deafness and Pili Torti, Bjornstad Type

73. Postgraduate Medicine: Return Of The Painful Leg Ulcers subungual splinter hemorrhages, blue toe syndrome, malignant atrophic papulosis,and porcelainwhite scars (ie, atrophie blanche) (1). http://www.postgradmed.com/issues/2002/04_02/puzzles_answer.htm

Return of the painful leg ulcers Ysabel M. Bello, MD; Tania J. Phillips, MD VOL 111 / NO 4 / APRIL 2002 / POSTGRADUATE MEDICINE Return to question The answer Antiphospholipid-antibody syndrome A ntiphospholipid-antibody syndrome (APS) is a multisystem disorder characterized by arterial or venous thrombosis, thrombocytopenia, recurrent fetal loss, and persistently elevated levels of antiphospholipid antibodies (1). Antiphospholipid antibodies are a heterogeneous group of circulating autoantibodies that includes anticardiolipin and anti-beta -glycoprotein I antibodies, which react with phospholipid-protein complexes, and lupus anticoagulants, which interfere with phospholipid-dependent coagulation reactions (2). APS may occur as either a primary disorder or a secondary disorder associated with (1) an underlying systemic disorder, including immunologic disease (most commonly systemic lupus erythematosus [SLE]), cancer, hematologic disease, infection, and neurologic disease, or (2) use of specific drugs (eg, procainamide hydrochloride, chlorpromazine hydrochloride and other phenothiazine derivatives, phenytoin, quinidine, streptomycin sulfate, clozapine) (1,2). Studies of patients with lupus anticoagulants have found that 50% of patients had SLE, while the remainder had various aforementioned disorders (1). Anticardiolipin antibodies are elevated in the presence of a diverse group of infectious agents, including HIV, whereas lupus anticoagulant in patients with HIV infection occurs more commonly with opportunistic infections and tends to disappear when the infection is treated (1).

74. : The AMEDEO Literature Guide Lesions resembling malignant atrophic papulosis in a patient with progressivesystemic sclerosis. Cutis 2005;751014. PubMed Related articles Abstract http://www.amedeo.com/medicine/skd/skd3.htm

Home HIV Medicine FAQ Unsubscribe ... Flying Publisher Dermatology Free Subscription Am J Pathol Ann Intern Med Cancer ... Text format Single Articles Am J Pathol SATOH T , Kanai Y, Wu MH, Yokozeki H, et al Am J Pathol 2005;167:787-96. PubMed Related articles Abstract available BAMBERGER C , Scharer A, Antsiferova M, Tychsen B, et al Activin Controls Skin Morphogenesis and Wound Repair Predominantly via Stromal Cells and in a Concentration-Dependent Manner via Keratinocytes. Am J Pathol 2005;167:733-47. PubMed Related articles Abstract available DE GIORGIO-MILLER A , Bottoms S, Laurent G, Carmeliet P, et al Fibrin-induced skin fibrosis in mice deficient in tissue plasminogen activator. Am J Pathol 2005;167:721-32. PubMed Related articles Abstract available Ann Intern Med ROBERT C , Faivre S, Raymond E, Armand JP, et al Subungual splinter hemorrhages: a clinical window to inhibition of vascular endothelial growth factor receptors? Ann Intern Med 2005;143:313-4. PubMed Related articles Cancer GUTH U , Wight E, Schotzau A, Langer I, et al Breast carcinoma with noninflammatory skin involvement (T4b).

75. Cutis Lesions Resembling malignant atrophic papulosis in a Patient With ProgressiveSystemic Sclerosis Liu CM, Harris RM, Hansen CD Abstract PDF http://www.cutis.com/asp/archive/pasttoc.asp?issuemonth=2&issueyear=2005

76. The American Journal Of The Medical Sciences - UserLogin presentation of HIV infection, 3 and malignant atrophic papulosis, which causesinfarctive thrombosis of the skin and viscera, has been reported. http://www.amjmedsci.com/pt/re/ajms/fulltext.00000441-200012000-00005.htm

LWWOnline LOGIN eALERTS REGISTER ... Archive You are attempting to access protected content. To access this content please login using an established account or create/activate an account. If you have already created/ activated an online account, please login below: User Name: Password: Note: passwords are CASE SENSITIVE If you are a new user or guest visiting an LWWonline site for the first time, please complete the new account setup process to view or purchase content. Forgot your password? Subscribe Renewal Information Subscribe to RSS feed utrdc-pt01 Release 4.0

77. Rare Pediatric Disease Database malignant atrophic papulosis, Progressive arterial occlusive disease, Benigncutaneous Degos syndrome, Degos syndrome. Document created on 2/3/2004 http://www.madisonsfoundation.org/content/3/1/display.asp?did=394

78. MUMS List Of Disorders - M malignant atrophic papulosis(Degos disease) www.degosdisease.com; MalignantHyperthermia (12) *; Malrotation of the Intestines (31) http://www.netnet.net/mums/mum_m.htm

Return to MUMS Home Page MUMS: List of Disorders M Number in parentheses indicates number of matches. indicates there is a support group which covers that diagnosis. MELAS Mitochondrial Encephalopathy Lactic Acidosis Syndrome (7) * Macrocephaly (large head) (29) http://www.macrocephaly-cmtc.com/ Macrodactyly (Large toes or fingers) (2) Macroglossia (6) Macrosomia (abnormally large body) (2) Macular Degeneration (4) * Macular Degeneration (Infantile) * Male Pseudohermaphroditism (2) * Malignant Atrophic Papulosis(Degos disease) www.degosdisease.com Malignant Hyperthermia (12) * Malrotation of the Intestines (31) Mandibuloacral Dysplasia(Craniomandibular Dermatodysostis) (3) Manic Depression, Bipolar (64) * Manic Depressive Schizophrenia (19) * Mannosidosis (Glycogen Storage) (4)** Maple Syrup Urine Disease (7) * Marcus Gunn Phenomenon (Jaw Winking) (3) Marden-Walker Syndrome (7) Marfan Syndrome (12) * Marinesco-Sjogren Syndrome (1) www.marinesco-sjogren.org Marshall-Smith Syndrome (1) Mast Cell Disease (Urticaria Pigmentosa) (9) Mastocytosis (Urticaria Pigmentosa) (9) www.mastokids.org

79. MUMS List Of Disorders - D - E Bjornstad Type (1); Degos disease (malignant atrophic papulosis)www.degosdisease.com; DejerineSottas Disease (Sensory Motor Neuropathy III) (6)* http://www.netnet.net/mums/mum_d-e.htm

Return to MUMS Home Page MUMS: List of Disorders D - E Number in parentheses indicates number of matches. indicates there is a support group which covers that diagnosis. D-2Hydroxyglutaric Aciduria (2) DOORS Syndrome (4) DPT (damage from vaccine) (306) * Dandy-Walker Syndrome (68) * Darier Disease (1) * Darrow-Gamble Syndrome(Congenital Chloride Diarrhea) (1) * De Barsy Syndrome (lacking elasticity in skin) (2) DeMorisier Dysplasia Olfactorgenitalis (Kallmann Syndrome) (5) * Deaf/Blindness (71) * www.deafblindinfo.org Deaf/Blindness from Polio Vaccine (1) * Deafness (195) * Deafness-Pili-Torti, Bjornstad Type (1) Degos disease (Malignant Atrophic Papulosis) www.degosdisease.com Dejerine-Sottas Disease (Sensory Motor Neuropathy III) (6)* Delleman-Oorthuys Syndrome (1) Dentatorubral-Pallidoluysian Atrophy (DRPLA) (1) Dermatitis, Atopic (1) Dermatomyositis (15) * Desanctis-Cacchione Syndrome (Xeroderm Pigmentosum) (7) Developmentally Delayed (2735) * http://groups.yahoo.com/group/childdevdelays/ Dextrocardia (heart on right side) (34) * Dextrocardia with Situs Inversus (organs backward) (13) Dextrocardia-Bronchiectasis-Sinusitis Syndrome (Kartagener) (11) DiGeorge Syndrome (49) ** DiGeorge Syndrome and Klinefelter Syndrome (1) Diabetes, Gestational (5) *

80. Vasculitis Degos Disease is a rare disease, also known as malignant atrophic papulosis,initially presenting as a skin condition characterised by red papules with http://omni.ac.uk/browse/mesh/D014657.html

low graphics Vasculitis 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 Last modified: 09 Sep 2005

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 4     61-80 of 98    Back | 1  | 2  | 3  | 4  | 5  | Next 20