Gardner’s Syndrome- Clinical Manifestation Of A Rare Syndrome

Gardner's syndrome is a variant of familial adenomatous polyposis. This syndrome is characterized by multiple intestinal polyposis, osteomas, and epidermoid cysts. In addition, dental abnormalities include an increased frequency of multiple odontomas, supernumerary teeth and impacted teeth. The authors report the case of a 59-year-old male patient with Gardner syndrome. Radiographic findings revealed presence of osteoma in the frontal bone, multiple diffuse enostoses in both jaws and the presence of an epidermoid cyst on the scalp.