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Skin and Connective Tissue Diseases > Skin Diseases > Keratosis > Keratoderma, Palmoplantar > Papillon-Lefevre Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Keratoderma, Palmoplantar > Papillon-Lefevre Disease
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Keratoderma, Palmoplantar > Papillon-Lefevre Disease

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Papillon-Lefevre Disease  

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Tipo

  • mesh:Descriptor

Definición

  • 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. Mutations in the gene for CATHEPSIN C have been associated with this disease.

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Keratosis Palmoplantar Periodontopathy
  • Keratosis Palmoplantaris with Periodontopathia
  • Papillon Lefevre Disease
  • Papillon-Lefevre Syndrome

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-R4NMZL48-2

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