CHICAGO – January 30, 2003 – Canadian researchers found that patients with Kindler syndrome had an earlier onset of periodontitis and that the disease progressed more rapidly than in non-Kindler patients. Study findings were published in the January Journal of Periodontology.
Researchers believe Kindler syndrome is caused by an unidentified genetic disorder that gives the appearance of two congenital diseases of the skin, epidermolysis bullosa dystrophia and poikilodoerma. Epidermolysis bullosa dystrophia is a condition in which the skin and mucous membranes are fragile. Any friction or trauma to skin and/or mucous membranes causes blisters and the skin to come off. Poikiloderma is a condition characterized by pigmentary and atrophic changes in the skin, giving skin a spotted appearance.
The study looked at 31 patients (18 with Kindler syndrome and 13 without) from rural Panama to determine the extent to which periodontal disease is associated with Kindler syndrome.
"The major finding of this study was that individuals with Kindler syndrome develop periodontitis at an earlier age and the disease progresses rapidly," said Colin
Definition criteria for periodontitis in this study was clinical attachment loss (CAL) of at least
Kindler patients had an average CAL of 6 mm by age 20, while it was estimated to take
"Previous studies have suggested a link between periodontal disease and Kindler syndrome, but this study confirms the risk these patients have for developing periodontitis at a much younger age than a dentist would normally expect," said
He continued, "Of considerable interest is the additional information that can be learned about the relationship of periodontal disease and the genetic defect of these patients. Once the defect has been identified, we can take the information and apply it to other patients who are genetically predisposed to periodontal disease, which may help us determine positive treatment outcomes for periodontal disease."
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