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This paper presents treatment planning and follows up of 6 year of a child patient with Papillon Lefevre syndrome. Papillon Lefevre syndrome is a rare autosomal recessive syndrome that is characterized by palmoplanar hyperkeratozis and premature loss of tooth. As the result of clinical, immunological and hematological findings, the child patient was diagnosed as having PLS at 2005. The treatment consisting of extraction of all primary teeth at general anesthesia. After an edentulous period complete denture were inserted. And when permanent teeth were erupted, the denture was modified. Treatment procedure was continued with the distal screw with removal appliance. The patient is still under control.
Field : Sağlık Bilimleri
Journal Type : Uluslararası
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