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8 wrz 2022 · Gardner syndrome is a rare, inherited condition where people develop hundreds and sometimes thousands of abnormal growths in their large and small intestines. These growths, called polyps, are noncancerous at first, but some have an almost 100% chance of becoming cancerous.
Gardner syndrome symptoms change over time. People with this condition may develop symptoms as children, including: Noncancerous tumors in bones or soft tissues. Dental issues, such as having extra teeth. Multiple colon polyps are a common Gardner syndrome symptom.
Other signs and symptoms of Gardner syndrome include dental abnormalities; osteomas (benign bone growths); various skin abnormalities such as epidermoid cysts, fibromas (a benign tumor of the connective tissue), and lipomas; and desmoid tumors.
Gardner syndrome is a variant of familial adenomatous polyposis (FAP) that is associated with extra-colonic features. It is an inherited disease that is characterised by gastrointestinal polyps, multiple osteomas (benign bone tumours), and various skin and soft tissue tumours.
Gardner's syndrome (also known as Gardner syndrome, familial polyposis of the colon, [1] or familial colorectal polyposis [2]) is a subtype of familial adenomatous polyposis (FAP). Gardner syndrome is an autosomal dominant form of polyposis characterized by the presence of multiple polyps in the colon together with tumors outside the colon. [ 3 ]
30 sty 2023 · Gardner syndrome is a rare genetic condition where abnormal growths, called polyps, develop in the large intestine. There is no cure for Gardner syndrome. However, regular screening and...
13 kwi 2023 · Gardner’s syndrome is a genetic disorder that is characterized by intestinal polyps and dental anomalies. Learn the causes, symptoms, diagnosis, treatment, and life expectancy of GS.
