Literature DB >> 18454678

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

Colin B Wiebe1, Giorgio Petricca, Lari Häkkinen, Guoqiao Jiang, Chuanyue Wu, Hannu S Larjava.   

Abstract

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.

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Year:  2008        PMID: 18454678      PMCID: PMC2697853          DOI: 10.1902/jop.2008.070167

Source DB:  PubMed          Journal:  J Periodontol        ISSN: 0022-3492            Impact factor:   6.993


  29 in total

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4.  Clinical and microbiologic study of periodontitis associated with Kindler syndrome.

Authors:  Colin B Wiebe; Homero Penagos; Nancy Luong; Jørgen Slots; Ervin Epstein; Dawn Siegel; Lari Häkkinen; Edward E Putnins; Hannu S Larjava
Journal:  J Periodontol       Date:  2003-01       Impact factor: 6.993

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Authors:  Dawn H Siegel; Gabrielle H S Ashton; Homero G Penagos; James V Lee; Heidi S Feiler; Kirk C Wilhelmsen; Andrew P South; Frances J D Smith; Alan R Prescott; Vesarat Wessagowit; Noritaka Oyama; Masashi Akiyama; Daifullah Al Aboud; Khalid Al Aboud; Ahmad Al Githami; Khalid Al Hawsawi; Abla Al Ismaily; Raouf Al-Suwaid; David J Atherton; Ruggero Caputo; Jo-David Fine; Ilona J Frieden; Elaine Fuchs; Richard M Haber; Takashi Harada; Yasuo Kitajima; Susan B Mallory; Hideoki Ogawa; Sedef Sahin; Hiroshi Shimizu; Yasushi Suga; Gianluca Tadini; Kikuo Tsuchiya; Colin B Wiebe; Fenella Wojnarowska; Adel B Zaghloul; Takahiro Hamada; Rajeev Mallipeddi; Robin A J Eady; W H Irwin McLean; John A McGrath; Ervin H Epstein
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Authors:  M Redlich; E Reichenberg; D Harari; B Zaks; S Shoshan; A Palmon
Journal:  J Dent Res       Date:  2001-12       Impact factor: 6.116

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Authors:  T Maffucci; M Falasca
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Journal:  Biochim Biophys Acta       Date:  2003-04-17
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Journal:  EMBO Rep       Date:  2008-11-07       Impact factor: 8.807

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Review 7.  New perspectives on amelotin and amelogenesis.

Authors:  J D Bartlett; J P Simmer
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Review 8.  Oral manifestations in the epidermolysis bullosa spectrum.

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Journal:  Spec Care Dentist       Date:  2020-11

10.  Comparison of periodontal parameters in individuals with syndromic craniosynostosis.

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