Fogorvosi szemle, 2009 (102. évfolyam, 1-6. szám)
2009-06-01 / 3. szám
FOGORVOSI SZEMLE 102. évf. 3. sz. 2009. 95 80. Page RC, Beatty P, Waldrop TC: Molecular basis for the functional abnormality in neutrophils from patients with generalized prepubertal periodontitis. J Periodontal Res 1987; 22: 182-183. 81. Pernu HE, Pajari UH, Lanning M: The importance of regular dental treatment in patients with cyclic neutropenia. Follow-up of 2 cases. J Periodontol 1996; 67: 454-459. 82. Pham CT, Ivanovich JL, Raptis SZ, Zehnbauer B, Ley TJ: Papillon-Lefèvre syndrome: correlating the molecular, cellular, and clinical consequences of cathepsin C/dipeptidyl peptidase I deficiency in humans. J Immunol 2004; 173(12): 7277-7281. 83. Pinkerton PH, Robinson JB, Senn JS: Lazy leucocyte syndromedisorder of the granulocyte membrane? J Clin Pathol 1978; 31: 300- 308. 84. Reichart PA, Dornow H: Gingivo-periodontal manifestations in chronic benign neutropenia. J Clin Periodontol 1978; 5: 74-80. 85. 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Watanabe K: Prepubertal periodontitis: a review of diagnostic criteria, pathogenesis, and differential diagnosis. J Periodontal Res 1990; 25: 31-48. Review. 102. Wiebe Cb, Silver Jg, Larjava Hs: Early-onset periodontitis associated with Weary-Kindler syndrome: a case report. J Periodontol 1996; 67(10): 1004-1010. 103. Yakubenia S, Wild Mk: Leukocyte adhesion deficiency II. Advances and open questions. FEBS J. 2006; 273: 4390-4398. Review. 104. Yeowell Hn, Pinnell Sr: The Ehlers-Danlos syndromes. Semin Dermatol 1993; 12: 229-240. Review 105. Zaromb A, Chamberlain D, Schoor R, Almas K, Blei F: Periodontitis as a manifestation of chronic benign neutropenia. J Periodontol 2006; 77: 1921-1926. Dr. Gera I, Dr. Vári M: Genetic background of periodontitis Part I. Basic principles and syndromes with Mendelian inheritance Review of literature Periodontitis is an infectious disease. It had previously been considered as a diseases caused merely by the dental plaque. During the nineteen-nineties a substantial number of publications indicated the role of other risk factors in the pathogenesis-like behavioural, systemic and genetic ones. Based on the recent research data the genetic factors and the ethnicity have become one of the leading susceptibility or severity factors for destructive periodontitis. The family background of early onset aggressive periodontitis has long been known. Hereditary syndromes can very frequently be associated with severe periodontitis. Both facts can support the alleged connection between certain genes’ mutation and periodontal manifestation. Periodontal disease associated with systemic hereditary syndromes mainly shows a Mendelian inheritance. The locus and the characteristics of the gene mutations have in many cases been identified. Nevertheless several polygenic gene single nucleotide mutations can also be a predisposing or severity factor for periodontitis. Part I of the literature review is focusing on those syndromes in which major PMN leukocyte deficiency or dysfunction or certain structural protein deficiency occur. Key words: periodontitis, Mendelian inheritance, gene mutation, inherited syndromes, leukocyte deficiencies