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- W2893423543 abstract "Gardner's syndrome is a rare autosomal dominant disease characterized by intestinal polyposis, connective tissue tumors, and multiple osteomatosis. A 14-year-old boy reported a complaint of a 1-year duration, painless, bilateral face swelling. Radiographic investigations revealed a circumscribed, radiopaque lesion in the posterior region of the left base of the mandible, 0.5 cm in diameter, compatible with osteoma. Initially, a clinico-radiographic follow-up was conducted. However, as the panoramic radiograph showed a lesion enlargement owing to continuous osseous growth, an excisional biopsy was performed. The histopathological examination confirmed an osteoma diagnosis. A colonoscopy was also performed and showed multiple intestinal polyps, which were revealed to be tubular adenomas with mild dysplasia, in the histopathological examination. Sixteen years later, the patient is without oral complaints; however, recently, a total colectomy was performed due to multiple polyposis. This case reinforces the role of a dentist in the early diagnosis of Gardner's syndrome." @default.
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- W2893423543 date "2018-09-01" @default.
- W2893423543 modified "2023-10-16" @default.
- W2893423543 title "Gardner's Syndrome: a Case Report with 16 Years of Follow-Up" @default.
- W2893423543 doi "https://doi.org/10.1016/j.oooo.2018.02.446" @default.
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