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Hierarchy  - English - French - German - Spanish - Portuguese - Italian - Dutch    Papillon-Lefevre Disease Definition: Rare, autosomal recessive disorder occurring between the first and fifth years of life. It is characterized by palmoplantar keratoderma with periodontitis followed by the premature shedding of both deciduous and permanent teeth. Synonym(s): Papillon-Lefevre Syndrome / Disease, Papillon-Lefevre / Papillon Lefevre Disease / Papillon Lefevre Syndrome / MeSH 2010 © U.S. National Library of Medicine®. Browse - New search

Web resources for "Papillon-Lefevre Disease" = Site with HON description   -   = Site with a robot description info: enter the site: (click below) domain of the site:   Whonamedit - Papillon-Lefèvre syndrome www.whonamedit.com   HONcode - Orphanet: Papillon Lefèvre syndrome www.orpha.net 2 rare-diseases — National Organization for Rare Disorders www.rarediseases.org   Broader term(s): - Keratoderma, Palmoplantar - Skin Diseases, Genetic - Genetic Diseases, Inborn - Congenital, Hereditary, and Neonatal Diseases and Abnormalities Browse - New search       Medical image(s) for "Papillon-Lefevre Disease" No results for this term. Browse other medical images in HONmedia? Browse - New search       Medical News for "Papillon-Lefevre Disease" No results for this term. More health news Browse - New search       Scientific articles from MEDLINE for "Papillon-Lefevre Disease"   - English - French - German - Spanish - Portuguese - Italian - Dutch     All recent articles  Therapy:  by recall    /  by precision  Diagnosis:  by recall    /  by precision  Etiology:  by recall    /  by precision  Prognosis:  by recall    /  by precision Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy Browse - New search       Clinical Trials for "Papillon-Lefevre Disease" ClinicalTrials.gov - Linking patients to medical research Cytokines in Papillon-Lefèvre Syndrome Broader term(s): - Keratoderma, Palmoplantar - Congenital, Hereditary, and Neonatal Diseases and Abnormalities Browse - New search       Medical Conferences/Events for "Papillon-Lefevre Disease" No results for this term. Consult HON's world-wide database of medical meetings Browse - New search       Refine the search for  "Papillon-Lefevre Disease" Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy   Broader term(s):       Diseases           Skin and Connective Tissue Diseases               Skin Diseases                   Skin Diseases, Genetic                       Keratoderma, Palmoplantar                    Keratosis                       Keratoderma, Palmoplantar        Diseases           Congenital, Hereditary, and Neonatal Diseases and Abnormalities               Genetic Diseases, Inborn                   Skin Diseases, Genetic                       Keratoderma, Palmoplantar  MeSH 2010 © U.S. National Library of Medicine®. Browse - New search

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