Search results for "Papillon–Lefèvre syndrome"

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Cathepsin C gene: First compound heterozygous patient with Papillon-Lefèvre syndrome and a novel symptomless mutation.

2001

Papillon-Lefevre syndrome (PLS) has recently been shown to be caused by mutations in the cathepsin C gene resulting in periodontal disease and palmoplantar keratosis. Thirteen different homozygous mutations have been characterised in PLS patients of different ethnic origin. In the present paper, a PLS patient is described who carries two novel mutations (706G>T and 872G>A) in the paternal and maternal chromosomes, respectively. This is the first compound patient described so far. In addition, a novel symptomless mutation (458C>T) in the cathepsin C gene is described in three homozygous individuals. Thus, not all mutations should be considered as a cause of disease, whether case studies or g…

MaleHeterozygoteHaim–Munk syndromeDNA Mutational AnalysisMolecular Sequence DataMutation MissensePapillon–Lefèvre syndromeBiologyCompound heterozygositymedicine.disease_causePapillon-Lefevre DiseaseCathepsin CCathepsin CPapillon-Lefevre DiseaseGene FrequencyGeneticsmedicineHumansAlleleAllele frequencyAllelesGenetics (clinical)Family HealthGeneticsMutationDNAmedicine.diseaseMutationFemale
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Papillon- Lefevre Syndrome: Report of a case and its management

2012

Papillon-Lefèvre Syndrome (PLS) is a rare autosomal recessive disorder first described by two French physicians, Papillon and Lefèvre in 1924. The disorder is characterized by diffuse palmoplantar keratoderma and precocious aggressively progressing periodontitis, leading to the premature loss of deciduous and permanent teeth at a very young age. The cutaneous lesions are usually manifested simultaneously with the intra-oral presentations and include keratotic plaques on the palms and soles varying from mild psoriasiform scaly skin to overt hyperkeratosis. The etiopathogenesis of the syndrome is relatively obscure and immunologic, genetic or possible bacterial etiologies have been proposed. …

PeriodontitisPathologymedicine.medical_specialtybusiness.industryHyperkeratosisCase ReportOdontologíaPapillon–Lefèvre syndrome:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseScaly skinCiencias de la saludDiffuse palmoplantar keratodermaDermatologyYoung ageUNESCO::CIENCIAS MÉDICASmedicineEtiologyOdontostomatology for the Disabled or Special PatientsbusinessGeneral DentistryPermanent teethJournal of Clinical and Experimental Dentistry
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Papillon Lefevre syndrome: bridge between Dermatologist and Dentist

2010

Papillon-Lefevre syndrome is a rare autosomal recessively inherited condition which shows features common to both dentistry and dermatology. This disease is characterized by palmoplantar hyperkeratosis and severe periodon- titis. Therefore both the dentist and the dermatologist should be aware of the same because an early diagnosis of the syndrome can help to preserve the teeth by early institution of treatment, using a multidisciplinary approach. Here we present a case report of Papillon-Lefevre syndrome, along with a comprehensive review of the etiology, pathology, clinical features, differential diagnosis and management of the condition.

medicine.medical_specialtybusiness.industryDentistryOdontologíaPapillon–Lefèvre syndromeDiseasemedicine.disease:CIENCIAS MÉDICAS [UNESCO]DermatologySevere periodontitisCiencias de la saludUNESCO::CIENCIAS MÉDICASEtiologymedicineDifferential diagnosisbusinessGeneral Dentistry
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