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Multidisipliner yaklaşım ile papillon lefevre sendromu: 6 yıllık takip

Papillon lefevre syndrome with multidisciplinar approach: 6 years follow–up

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Abstract (2. Language): 
This paper presents treatment planning and 6 years follow–up of a patient with Papillon Lefevre syndrome (PLS). Papillon Lefevre syndrome is a rare autosomal recessive syndrome characterized by palmoplantar hyperkeratozis and premature tooth loss. As a result of clinical, immunological and hematological findings, the patient referred to our department in 2005,was diagnosed as PLS. The preliminary phase of the treatment consisted of extraction of all primary teeth under general anaesthesia. Following the edentulous period, a removable denture was delivered. The denture was modified as permanent teeth erupted. Additively, removal appliance with distal screw was applied. The patient is still under maintenance.
Abstract (Original Language): 
Papillon Lefevre sendromlu (PLS) bir çocuk hastanın 6 yıllık tedavi ve takip süreci sunulmuştur. Papillon Lefevre sendromu, palmoplantar hiperkeratoz ve dişlerin erken kaybı ile karakterize, nadir görülen otozomal resesif bir hastalıktır. 2005 yılında kliniğimize yönlendirilen çocuk hastaya klinik, immunolojik ve hematolojik bulguların sonucunda hastaya PLS teşhisi konulmuştur. Tedavinin ilk aşamasında genel anestezi altında bütün süt dişleri çekilmiştir. Dişsiz periyodu takiben hastaya çocuk protezi uygulaması yapılmış ve daimi dişler sürmeye başladıkça protezi modifiye edilmiştir. Ayrıca distal vidalı verenli müteharik aparey ile yer açma tedavisine başlanmıştır. Hasta rutin kontrollerine devam etmektedir
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