Kindler syndrome and periodontal disease:: Review of the literature and a 12-year follow-up case

被引:2
作者
Wiebe, Colin B. [1 ]
Petricca, Giorgio [1 ]
Hakkinen, Lari [1 ]
Jiang, Guoqiao [1 ]
Wu, Chuanyue [1 ]
Larjava, Hannu S. [1 ]
机构
[1] Univ British Columbia, Fac Dent, Dept Oral Biol & Med Sci, Vancouver, BC V6T 1Z3, Canada
关键词
case report; kindlin-1; periodontitis; treatment outcome;
D O I
10.1902/jop.2008.070167
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: The association of aggressive periodontitis with Kindler syndrome was based on a single case in 1996 and later confirmed with a larger population. Since then, significant research has greatly increased our understanding of the molecular pathology of this disorder. We review recent advances in the molecular mechanisms of the syndrome and present a maintenance case report of a patient who has been followed in our clinic. Methods: A female patient who was diagnosed with Kindler syndrome and aggressive periodontitis at the age of 16 years has been followed and treated in our clinic for 12 years. Her main treatment has been maintenance therapy following her initial treatment and restorative work previously documented. Gingival biopsies obtained during the recent extraction of hopeless maxillary molars were used for histologic assessment of gingival tissue attachment apparatus and to isolate gingival fibroblasts. Reverse transcription-polymerase chain reaction (RT-PCR) was performed using these cells to confirm the lack of expression of kindlin-1. Results: RT-PCR showed the total loss of kindlin-1 mRNA in cultured gingival fibroblasts, supporting the clinical diagnosis of Kindler syndrome. Tissue biopsies revealed atypical pocket epithelium. Maintenance therapy has been moderately successful. Teeth that were recently lost had a poor prognosis at the initial assessment. The patient's gingiva and oral mucosa continue to be fragile with episodes of sloughing and inflammation. Conclusions: Periodontitis in Kindler syndrome responds to maintenance therapy, but the gingiva and oral mucosa continue to display an abnormal appearance with white patches. Histologic findings suggest that the junctional epithelium in Kindler syndrome may be abnormal and could explain why these patients have periodontal disease. Attachment loss progressed around teeth with an initial guarded or poor prognosis. Teeth that started with a good or fair prognosis continue to have a fair prognosis. Limited dental implant treatment is being considered.
引用
收藏
页码:961 / 966
页数:6
相关论文
共 29 条
  • [1] Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome
    Ashton, GHS
    McLean, WHI
    South, AP
    Oyama, N
    Smith, FJD
    Al-Suwaid, R
    Al ismaily, A
    Atherton, DJ
    Harwood, CA
    Leigh, IM
    Moss, C
    Didona, B
    Zambruno, G
    Patrizi, A
    Eady, RAJ
    McGrath, JA
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 122 (01) : 78 - 83
  • [2] Kindler syndrome
    Ashton, GHS
    [J]. CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2004, 29 (02) : 116 - 121
  • [3] The talin head domain binds to integrin β subunit cytoplasmic tails and regulates integrin activation
    Calderwood, DA
    Zent, R
    Grant, R
    Rees, DJG
    Hynes, RO
    Ginsberg, MH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (40) : 28071 - 28074
  • [4] The phosphotyrosine binding-like domain of talin activates Integrins
    Calderwood, DA
    Yan, BX
    de Pereda, JM
    Alvarez, BG
    Fujioka, Y
    Liddington, RC
    Ginsberg, MH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) : 21749 - 21758
  • [5] KINDLER SYNDROME - REPORT OF 2 CASES AND REVIEW OF THE LITERATURE
    FORMAN, AB
    PRENDIVILLE, JS
    ESTERLY, NB
    HEBERT, AA
    DUVIC, M
    HORIGUCHI, Y
    FINE, JD
    [J]. PEDIATRIC DERMATOLOGY, 1989, 6 (02) : 91 - 101
  • [6] Molecular basis of Kindler syndrome in Italy:: Novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene
    Has, Cristina
    Wessagowit, Vesarat
    Pascucci, Monica
    Baer, Corinna
    Didona, Biagio
    Wilhelm, Christian
    Pedicelli, Cristina
    Locatelli, Andrea
    Kohlhase, Juergen
    Ashton, Gabrielle H. S.
    Tadini, Gianluca
    Zambruno, Giovanna
    Bruckner-Tuderman, Leena
    McGrath, John A.
    Castiglia, Daniele
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (08) : 1776 - 1783
  • [7] Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes
    Herz, Corinna
    Aumailley, Monique
    Schulte, Carsten
    Schloertzer-Schrehardt, Ursula
    Bruckner-Tuderman, Leena
    Has, Cristina
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (47) : 36082 - 36090
  • [8] Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome
    Jobard, F
    Bouadjar, B
    Caux, E
    Hadj-Rabia, S
    Has, C
    Matsuda, E
    Weissenbach, J
    Lathrop, M
    Prud'homme, JF
    Fischer, J
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 (08) : 925 - 935
  • [10] The kindler syndrome protein is regulated by transforming growth factor-β and involved in integrin-mediated adhesion
    Kloeker, S
    Major, MB
    Calderwood, DA
    Ginsberg, MH
    Jones, DA
    Beckerle, MC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (08) : 6824 - 6833