Gardner syndrome associated with multiple osteomas, intestinal polyposis, and epidermoid cysts
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چکیده
منابع مشابه
Gardner syndrome associated with multiple osteomas, intestinal polyposis, and epidermoid cysts
Gardner syndrome is known as a variant of familial adenomatous polyposis. This syndrome is characterized by multiple intestinal polyposes, osteomas, and epidermoid cysts. In addition, dental abnormalities include an increased frequency of multiple odontomas, as well as supernumerary and impacted teeth. The authors report the case of a 7-year-old male patient with Gardner syndrome. Radiographic ...
متن کاملCASE REPORT The concomitant occurrence of multiple epidermal cysts, osteomas and thyroid gland nodules is not diagnostic for Gardner syndrome in the absence of intestinal polyposis: a clinical and genetic report
*Institute of Clinical Pharmacology and Toxicology, Department of Clinical Pharmacology, and Department of Dermatology, University Medical Center Benjamin Franklin, Freie Universität Berlin, Fabeckstrasse 60–62, 14195 Berlin, Germany Institute of Pharmacology, Toxicology and Natural Products, Department of Pharmacology of Natural Products and Clinical Pharmacology, University of Ulm, Ulm, Germa...
متن کاملPEDIATRIC SURGERY Update
Gardner=s syndrome refers to a group of children born with familial adenomatous (multiple) polyposis and significant extracolonic manifestations. Familial adenomatous polyposis is an autosomal dominant disorder originating from a germline alteration of the adenomatous polyposis coli gene in the long arm of chromosome 5. The most significant extracolonic manifestation of Gardner=s syndrome consi...
متن کاملIntestinal polyposis associated with melanosis oris.
Weber (1919) described a case of acute intussusception in one of a pair of twins originally noticed by Hutchinson (1896) to have oral pigmentation. Peutz (1921) recorded a family of seven, and Jeghers, McKusick and Katz (1949) reported 10 cases of melanosis of the lips and buccal mucosa together with polyposis of the gastro-intestinal tract. The latter's report included a review of the literatu...
متن کاملGardner's syndrome with bilateral osteomas of coronoid process resulting in limited opening.
Gardner’s syndrome is characterized by a triad of intestinal polyposis, which ultimately become malignant, soft-tissue neoplasms such as desmoid tumors and fibromas, and osteomas, particularly of the skull and facial bones. A case report of bilateral osteomas of the coronoid process resulting in limited incisal opening in a 12-year-old girl and review of the pertinent literature is presented. G...
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ژورنال
عنوان ژورنال: Imaging Science in Dentistry
سال: 2016
ISSN: 2233-7822,2233-7830
DOI: 10.5624/isd.2016.46.4.267