Papillon-lefevre syndrome: an unusual case report
Papillon-Lefevre syndrome (PLS) is a rare autosomal disorder characterized by palmoplantar hyperkeratosis and periodontal problems leading to premature loss of both primary and permanent dentitions. It is caused by mutation of cathepsin C gene generating deficiency in host immune response to microor...
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| Veröffentlicht in: | International journal of dental clinics 2015-07, p.28 |
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| creator | Ozkan, Gokhan Kanli, Aydan Halici, Saniye Eren |
| description | Papillon-Lefevre syndrome (PLS) is a rare autosomal disorder characterized by palmoplantar hyperkeratosis and periodontal problems leading to premature loss of both primary and permanent dentitions. It is caused by mutation of cathepsin C gene generating deficiency in host immune response to microorganisms. Up to date, no sexual or racial predominance has been detected. This paper report the diagnosis and rehabilitation procedures for a 14-year-old male patient with PLS . Keywords: Cathepsin C; hyperkeratosis; Papillon-Lefevre syndrome; prosthetic rehabilitation |
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It is caused by mutation of cathepsin C gene generating deficiency in host immune response to microorganisms. Up to date, no sexual or racial predominance has been detected. This paper report the diagnosis and rehabilitation procedures for a 14-year-old male patient with PLS . 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| ispartof | International journal of dental clinics, 2015-07, p.28 |
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| subjects | Care and treatment Diagnosis Dosage and administration Papillon-Lefevre disease Risk factors Sulfamethoxazole Trimethoprim |
| title | Papillon-lefevre syndrome: an unusual case report |
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