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Papillon Lefevre Syndrome- A Case Report Nirola Ashutosh*, Professor and HOD, Gupta Madhu, Professor, Singla Kanika, Senior Lecturer Address for Correspondence: Dr. Ashutosh Nirola, Professor and HOD, Department of Periodontology and Oral Implantology Luxmi Bai Institute of Dental Sciences and Hospital, Patiala, India
Online published on 7 December, 2011. Abstract Papillon Lefevre syndrome (PLS) is a rare autosomal recessive disease characterized by skin lesions which are manifested as palmar-plantar hyperkeratosis, severe periodontal destruction and precocious loss of teeth involving both the primary and permanent dentitions. PLS is caused by mutations in the cathepsin C gene located on chromosome 11 (11q14-q21). This report presents a 21 year old boy having the classic signs and symptoms of PLS. Top Keywords Papillon Lefevre Syndrome, Palmar -plantar keratosis, Cathepsin C gene, Aggressive periodontitis. Top | |
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