reduced results from

224 B

24 M

3 M

194

182

to ~69 options

options split into images, definition, symptoms, related diagnoses, diagnostic tests, therapies, and medications

category dental problems, dermatology, genetic or congenital frequency rare (U.S.)

likelihood by age

likelyhood by duration of symptoms

related physician types family practitioner internist dentist oral surgeon orthodontist postal code Find Local The results are computer generated suggestions to help you find a physician. MEDgle does not recommend any particular type of physician or claim to be complete or accurate in the providers and specialties suggested.

papillon lefevre syndrome - rare genetic disease affecting skin and teeth Definition for Papillon Lefevre Syndrome http://children.webmd.com/Papillon-Lefevre-Syndrome some common symptoms dental problems scaly patches on skin some related diagnoses 1 - 7 of 69 diagnoses drugs and toxins dental caries dental infections and other dental conditions dental abscess periodontitis temporomandibular joint dysfunction syphilis   more do i have 'Papillon Lefevre Syndrome'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'papillon lefevre syndrome' 1 - 1 of 1 diagnostic tests Dental panoramic radiography Papillon Lefevre Syndrome and Dental panoramic radiography therapeutic procedures for 'Papillon Lefevre Syndrome'? Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for Papillon Lefevre Syndrome: therapeutic procedure search results for 'papillon lefevre syndrome' 1 - 4 of 4 therapeutic procedures rankings are computer generated. please consult your health care provider. dental procedures Papillon Lefevre Syndrome and dental procedures Oral hygiene Papillon Lefevre Syndrome and Oral hygiene periodontal cleaning Papillon Lefevre Syndrome and periodontal cleaning dental care Papillon Lefevre Syndrome and dental care medications search results for 'papillon lefevre syndrome' 1 - 3 of 3 medications rankings are computer generated. please consult your health care provider.   acitretin Papillon Lefevre Syndrome and acitretin   isotretinoin Papillon Lefevre Syndrome and isotretinoin   Etretinate Papillon Lefevre Syndrome and Etretinate web search results for papillon lefevre syndrome Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - Papillon Lefevre Syndrome Orphanet: Papillon Lefevre syndrome Papillon-Lefevre syndrome. Orpha number. ORPHA678. Prevalence of rare ... The Papillon-Lefevre syndrome is psoriasiform hyperkeratosis of the palms and ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=678   www.orpha.net - summary Papillon-Lefevre syndrome - Wikipedia, the free encyclopedia Papillon-Lefevre syndrome has an autosomal recessive pattern of inheritance. Contents ... Keratosis palmoplantar periodontopathy; Papillon Lefevre Syndrome at NIH's ... http://en.wikipedia.org/wiki/Papillon-Lefevre_syndrome   en.wikipedia.org - summary Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations ... Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in ... many palmoplantar keratoderma (PPK) conditions, only Papillon-Lefèvre syndrome ... http://www.ncbi.nlm.nih.gov/pubmed/10662807   www.ncbi.nlm.nih.gov - summary Papillon Lefevre Syndrome - Yahoo! Health Important It is possible that the main title of the report Papillon Lefevre Syndrome is not the name you expected. Please check the synonyms listing to find the ... http://health.yahoo.com/children-resources/papillon-lefevre-...   health.yahoo.com - summary Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin ... Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin C gene. ... The Papillon-Lefèvre syndrome, inherited in an autosomal recessive pattern, ... http://www.ncbi.nlm.nih.gov/pubmed/11180012   www.ncbi.nlm.nih.gov - summary Papillon Lefevre Syndrome Important It is possible that the main title of the report Papillon Lefevre Syndrome is not the name you expected. ... http://www.webmd.com/children/Papillon-Lefevre-Syndrome   www.webmd.com - summary Papillon-Lefèvre syndrome: a successful outcome. 2005 Nov;76(11):1996-2001. Papillon-Lefèvre syndrome: a successful outcome. ... BACKGROUND: Papillon-Lefèvre syndrome (PLS) is a rare autosomal recessive ... http://www.ncbi.nlm.nih.gov/pubmed/16274321   www.ncbi.nlm.nih.gov - summary Papillon-Lefèvre syndrome and malignant melanoma. A high incidence of ... Papillon-Lefèvre syndrome (PLS) is a rare autosomal-recessive genodermatosis ... Papillon-Lefevre Disease/genetics. Skin Neoplasms/ethnology. Skin Neoplasms/etiology ... http://www.ncbi.nlm.nih.gov/pubmed/18401176?dopt=Abstract   www.ncbi.nlm.nih.gov - summary Encyclopedia P-Pz on Yahoo! Health Health encyclopedia of diseases and conditions covering symptoms, definitions, alternative names, causes, ... Papillon Lefevre Syndrome. Paracentesis ... http://health.yahoo.com/ency/p/   health.yahoo.com - summary WebMD Health A-Z - Find reliable health and medical information on ... Find a comprehensive index of trusted health and medical information. It is your ultimate guide to reliable ... Papillon Lefevre Syndrome. Papillotonic ... http://www.webmd.com/a-to-z-guides/health-topics/pa-pe.htm   www.webmd.com - summary HLA class I gene polymorphism in Iranian patients with Papillon-Lefevre ... HLA class I gene polymorphism in Iranian patients with Papillon-Lefevre Syndrome. ... BACKGROUND: Papillon-Lefevre Syndrome (PLS) is a rare autosomal recessive ... http://www.ncbi.nlm.nih.gov/pubmed/18057583   www.ncbi.nlm.nih.gov - summary Periodontitis: Common Dental Disorders: Merck Manual Professional ... syndrome; leukocyte adhesion deficiency syndromes; Papillon-Lefèvre syndrome; ... genetic agranulocytosis; Ehlers-Danlos syndrome (types IV and VIII); vitamin ... http://www.merck.com/mmpe/print/sec08/ch095/ch095e.html   www.merck.com - summary A family with Papillon-Lefevre syndrome reveals a requirement for ... A family with Papillon-Lefevre syndrome reveals a requirement for cathepsin C in ... Lefèvre syndrome (PLS), loss-of-function mutations in cathepsin C do not affect ... http://www.ncbi.nlm.nih.gov/pubmed/16410452   www.ncbi.nlm.nih.gov - summary Coenzyme Q10 - MayoClinic.com Mayo Clinic offers award-winning medical and health information and tools ... nutrition, obesity, Papillon-Lefevre Syndrome, physical performance, psychiatric ... http://www.mayoclinic.com/health/coenzyme-q10/NS_patient-coenzymeq10   www.mayoclinic.com - summary MedlinePlus Herbs and Supplements: Coenzyme Q10 Early study shows that CoQ10 may improve symptoms of chronic fatigue syndrome. ... nutrition, obesity, Papillon-Lefevre Syndrome, physical performance, psychiatric ... http://www.nlm.nih.gov/medlineplus/druginfo/natural/patient-coenzymeq10.html   www.nlm.nih.gov - summary Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region. Papillon-Lefevre syndrome (PLS) is an autosomal recessive disease which belongs ... Papillon-Lefevre Disease/genetics* Pedigree. Polymerase Chain Reaction ... http://www.ncbi.nlm.nih.gov/pubmed/9272739   www.ncbi.nlm.nih.gov - summary le site du projet Génodermatoses et Méditerranée Génodermatoses et Méditerranée -Se rencontrer pour mieux soigner ... Others: Kindler syndrome, Papillon-Lefèvre Syndrome, Chanarin Dorfamn Syndrome. ... http://asso.orpha.net/GM/cgi-bin/articles.php?lng=en&pg=26   asso.orpha.net - summary 2008 MeSH Tree Structures. C16 - Congenital, Hereditary, and Neonatal ... Gardner Syndrome [C16.131.077.393] Holoprosencephaly [C16.131.077.410] ... Papillon-Lefevre Disease [C16.320.850.475.600] Keratosis Follicularis [C16.320.850.490] ... http://www.nlm.nih.gov/mesh/trees2008/C16.html   www.nlm.nih.gov - summary Identification of cathepsin C mutations in ethnically diverse papillon ... ... C mutations in ethnically diverse papillon-Lefèvre syndrome patients. ... INTRODUCTION: Papillon-Lefèvre syndrome (PLS) is an autosomal recessive disorder ... http://www.ncbi.nlm.nih.gov/pubmed/11106356   www.ncbi.nlm.nih.gov - summary 2008 MeSH Tree Structures. C17 - Skin and Connective Tissue Diseases Papillon-Lefevre Disease [C17.800.428.435.600] Keratosis Follicularis [C17.800.428.452] ... LEOPARD Syndrome [C17.800.621.430.530.550.525] ... http://www.nlm.nih.gov/mesh/trees2008/C17.html   www.nlm.nih.gov - summary Orphanet: Dentin dysplasia ... disease, cyclic neutropenia, Chediak-Hegashi syndrome, histiocytosis X, Papillon-Lefevre syndrome), permanent teeth discolouration due to tetracyclines, Vitamin ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1653   www.orpha.net - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juillet ... de cohen 20 0.06% syndrome de marshall 20 0.06% trisomie 18 19 0.06 ... syndrome 3 0.01% otospongiose 3 0.01% papillon lefevre syndrome 3 ... http://orphanet.orpha.net/stat/orphanet/search_200607.html   orphanet.orpha.net - summary Evidence of a founder effect for four cathepsin C gene mutations in ... ... haplotype analysis of Papillon-Lefèvre syndrome probands that provides evidence ... in 32 families with Papillon-Lefèvre syndrome (PLS) and associated conditions. ... http://www.ncbi.nlm.nih.gov/pubmed/11158173   www.ncbi.nlm.nih.gov - summary Talk:Papillon-Lefevre syndrome - Wikipedia, the free encyclopedia Talk:Papillon-Lefevre syndrome. From Wikipedia, the free encyclopedia ... Retrieved from "http://en.wikipedia.org/wiki/Talk:Papillon-Lefevre_syndrome" ... http://en.wikipedia.org/wiki/Talk:Papillon-Lefevre_syndrome   en.wikipedia.org - summary Cathepsin C gene: First compound heterozygous patient with Papillon ... ... heterozygous patient with Papillon-Lefèvre syndrome and a novel symptomless mutation. ... Papillon-Lefèvre syndrome (PLS) has recently been shown to be caused by ... http://www.ncbi.nlm.nih.gov/pubmed/11180601   www.ncbi.nlm.nih.gov - summary 245000 http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=245000   www.ncbi.nlm.nih.gov - summary Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre ... Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome. ... Papillon-Lefèvre syndrome (PLS) is an autosomal recessive disorder characterised ... http://www.ncbi.nlm.nih.gov/pubmed/10593994   www.ncbi.nlm.nih.gov - summary Description of two new cathepsin C gene mutations in patients with ... ... of two new cathepsin C gene mutations in patients with Papillon-Lefèvre syndrome. ... BACKGROUND: Papillon-Lefèvre syndrome (PLS) is a rare autosomal disorder ... http://www.ncbi.nlm.nih.gov/pubmed/16460249   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Avril 2006 ... ... otopalatodigital syndrome 4 0.01% oxicefalia 4 0.01% papillon-lefevre 4 0.01 ... chronique 3 0.01% papas syndrome 3 0.01% papillon lefevre 3 0.01% paquidermia 3 ... http://www.orpha.net/stat/orphanet/search_200604.html   www.orpha.net - summary AceView: Gene:CTSC, a comprehensive annotation of human, mouse and worm ... AceView offers a comprehensive annotation of human, mouse and nematode genes ... Disease; papillon-lefevre syndrome; pals; Periodontitis; periodontitis, ... http://www.ncbi.nlm.nih.gov/IEB/Research/Acembly/av.cgi?db=h...   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Mai 2006 ... ... vitiligo 328 0.62% brugada syndrome 322 0.61% lupus 254 0.48% drepanocytose 219 ... 5 0.01% pancitopenia 5 0.01% papillon lefevre 5 0.01% pemphigoide 5 0.01 ... http://www.orpha.net/stat/orphanet/search_200605.html   www.orpha.net - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Avril 2007 ... ... kawasaki 151 0.20% capillary leak syndrome 149 0.20% holoprosencefalia 147 0.20 ... 18 0.02% osteoblastoma 18 0.02% papillon lefevre 18 0.02% parsonage turner 18 ... http://orphanet.orpha.net/stat/orphanet/search_200704.html   orphanet.orpha.net - summary MIM Gene map The OMIM Gene map presents the cytogenetic map location of disease genes and ... Papillon-Lefevre syndrome, 245000 (3); Haim-Munk syndrome, 245010(3) ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l245010   www.ncbi.nlm.nih.gov - summary Loss-of-function mutations in the cathepsin C gene result in ... Papillon-Lefèvre syndrome, or keratosis palmoplantaris with periodontopathia ... Papillon-Lefevre Disease/pathology. Pedigree. Point Mutation* Substances: DNA Primers ... http://www.ncbi.nlm.nih.gov/pubmed/10581027   www.ncbi.nlm.nih.gov - summary Proteolysis of macrophage inflammatory protein-1alpha isoforms LD78beta ... ... was confirmed by incubation with neutrophil lysates from Papillon-Lefevre ... periodontal tissue destruction in Papillon-Lefevre syndrome may be related to ... http://www.ncbi.nlm.nih.gov/pubmed/15728180   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juin 2006 ... ... 0.51% nanismo 216 0.50% brugada syndrome 175 0.41% síndrome de klinefelter 154 ... danlos 13 0.03% syndrome de gougerot sjogren 13 0.03% xantinuria 12 0.03 ... http://www.orpha.net/stat/orphanet/search_200606.html   www.orpha.net - summary Analysis of human leukocyte antigen class II gene polymorphism in ... ... polymorphism in Iranian patients with Papillon-Lefevre syndrome: a family study. ... BACKGROUND: Papillon-Lefevre syndrome (PLS) is a rare autosomal recessive ... http://www.ncbi.nlm.nih.gov/pubmed/18791284   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Octobre ... skull syndrome 10 0.02% colangiocarcinoma 10 0.02% cromosoma 17 10 0.02 ... pancreatitis cronica 4 0.01% pancreoblastoma 4 0.01% papillon lefevre 4 0.01 ... http://www.orpha.net/stat/orphanet/search_200610.html   www.orpha.net - summary Cathepsin C - Wikipedia, the free encyclopedia A family with Papillon-Lefevre syndrome reveals a requirement for cathepsin C in ... cathepsin C gene are responsible for Papillon-Lefèvre syndrome.". J. Med. ... http://en.wikipedia.org/wiki/Cathepsin_C   en.wikipedia.org - summary OMIM Update List for November, 1999 137580 GILLES DE LA TOURETTE SYNDROME; GTS ... 245000 PAPILLON-LEFEVRE SYNDROME; PALS. 269920 SIALIC ACID STORAGE DISEASE; SIASD ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?11.1999   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Janvier ... ... 0.15% polidactilia 73 0.14% brugada syndrome 72 0.14% ectrodactylie 72 0.14 ... syndrome 20 0.04% liposarkom 20 0.04% maladie de fabry 20 0.04% micropenis 20 ... http://www.orpha.net/stat/orphanet/search_200701.html   www.orpha.net - summary NCBI CDD cd02621 CDD is a protein domain classification resource of the National Center for ... Papillon-Lefevre syndrome: correlating the molecular, cellular, and clinical ... http://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?ascbin=...   www.ncbi.nlm.nih.gov - summary AP Read - NextBio Papillon-Lefèvre syndrome, or keratosis palmoplantaris with periodontopathia ... cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and ... http://www.nextbio.com/b/literature/literature.nb?author=AP+Read   www.nextbio.com - summary Cysteine proteases as disease markers. This review comprises issues concerning cysteine cathepsins (CCs): human ... gene mutation and Papillon-Lefevre and Haim-Munk syndrome caused by catC gene defect. ... http://www.ncbi.nlm.nih.gov/pubmed/15026265   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Fevrier ... ... syndrome de klinefelter 56 0.10% biliary atresia 56 0.10% cornelia de lange 56 ... 9 0.02% ostéosclérose 9 0.02% papillon lefevre 9 0.02% paraganglioma 9 0.02 ... http://www.orpha.net/stat/orphanet/search_200702.html   www.orpha.net - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Juin 2007 ... syndrome 34 0.02% carcinoma nasofaringeo 34 0.02% demodicidosis 34 0.02% factor ... papillon lefevre 8 0.01% sindrome de rieger 8 0.01% sindrome de rotor 8 0.01 ... http://www.orpha.net/stat/orphanet/search_200706.html   www.orpha.net - summary Keratoderma - Wikipedia, the free encyclopedia Papillon-Lefèvre syndrome. Pachyonychia congenita type I. Pachyonychia congenita type II ... Vohwinkel syndrome. Palmoplantar keratoderma associated with ... http://en.wikipedia.org/wiki/Keratoderma   en.wikipedia.org - summary OMIM Update List for November, 2001 245000 PAPILLON-LEFEVRE SYNDROME; PALS. 249100 FAMILIAL MEDITERRANEAN FEVER; FMF ... Synopsis for 245000 PAPILLON-LEFEVRE SYNDROME; PALS. November 2, 2001 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?11.2001   www.ncbi.nlm.nih.gov - summary Statistique d'Usage du Serveur Orphanet orphanet.orpha.net - Aout 2007 ... ... 12 0.01% papillon lefevre 12 0.01% parsonage-turner syndrome 12 0.01% penis ... sindrome de marshall 11 0.01% sindrome de papillon lefevre 11 0.01% sindrome de ... http://www.orpha.net/stat/orphanet/search_200708.html   www.orpha.net - summary OMIM Update List for November, 2003 Clinical Synopsis for 153300 YELLOW NAIL SYNDROME ... 180860 SILVER-RUSSELL SYNDROME; SRS ... 245000 PAPILLON-LEFEVRE SYNDROME; PALS. 245010 HAIM-MUNK SYNDROME; HMS ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?11.2003   www.ncbi.nlm.nih.gov - summary show more 1  2