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      Papillon Lefevre syndrome.

      The Journal of the Association of Physicians of India
      Adolescent, Cathepsin C, genetics, Ceftriaxone, administration & dosage, therapeutic use, Chromosomes, Human, Pair 11, Genes, Recessive, Gentamicins, Humans, Keratoderma, Palmoplantar, Liver Abscess, Pyogenic, Male, Mutation, Papillon-Lefevre Disease, drug therapy, Periodontal Diseases

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          Abstract

          Papillon Lefèvre syndrome is a rare disease characterized by skin lesions caused by palmar-plantar hyperkeratosis, and severe periodontal destruction involving both the primary and permanent dentitions. It is transmitted as an autosomal recessive condition and consanguinity of parents is evident in about one-third of cases. Pyogenic liver abscess is an increasingly recognized complication. We report a new case of this association and review the current literature.

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