مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

CASE REPORT: PAPILLON-LEFEVRE SYNDROME

Pages

  33-38

Abstract

 Introduction: Papillon-Lefevre syndrome (PLS) characterized by PALMOPLANTAR hyperkeratosis is a rare autosomal recessive genetic disorder with rapidly progressive PERIODONTITIS and premature loss of both deciduous and permanent teeth. In this study, we report the clinical and radiographic features of Papillon-Lefevre syndrome in an 11- year-old girl and we also discuss the history and various theories about the etiology and treatment planning for this syndrome.

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  • Cite

    APA: Copy

    BASIRAT, MARYAM, PAKFETRAT, ATESSA, & JAVADIAN LANGAROODI, ADINEH. (2013). CASE REPORT: PAPILLON-LEFEVRE SYNDROME. JOURNAL OF DENTOMAXILLOFACIAL RADIOLOGY, PATHOLOGY AND SURGERY, 1(2), 33-38. SID. https://sid.ir/paper/331559/en

    Vancouver: Copy

    BASIRAT MARYAM, PAKFETRAT ATESSA, JAVADIAN LANGAROODI ADINEH. CASE REPORT: PAPILLON-LEFEVRE SYNDROME. JOURNAL OF DENTOMAXILLOFACIAL RADIOLOGY, PATHOLOGY AND SURGERY[Internet]. 2013;1(2):33-38. Available from: https://sid.ir/paper/331559/en

    IEEE: Copy

    MARYAM BASIRAT, ATESSA PAKFETRAT, and ADINEH JAVADIAN LANGAROODI, “CASE REPORT: PAPILLON-LEFEVRE SYNDROME,” JOURNAL OF DENTOMAXILLOFACIAL RADIOLOGY, PATHOLOGY AND SURGERY, vol. 1, no. 2, pp. 33–38, 2013, [Online]. Available: https://sid.ir/paper/331559/en

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