multiple familial polyposis oor Spaans

multiple familial polyposis

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poliposis grueso

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In an animal model of familial adenomatous polyposis (FAP), treatment with two other thiazolidinediones increased tumour multiplicity in the colon
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In an animal model of familial adenomatous polyposis (FAP), treatment with two other thiazolidinediones increased tumour multiplicity in the colon
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In an animal model for familial adenomatous polyposis (FAP), treatment with rosiglitazone at # times the pharmacologically active dose increased tumour multiplicity in the colon
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In an animal model for familial adenomatous polyposis (FAP), treatment with rosiglitazone at # times the pharmacologically active dose increased tumour multiplicity in the colon
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Certain inherited genetic syndromes – Genetic syndromes like familial medullary thyroid cancer, multiple endocrine neoplasia and familial adenomatous polyposis may increase your risk of thyroid cancer.
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Multiple polyps may represent familial adenomatous polyposis.
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People with the classic type of familial adenomatous polyposis may begin to develop multiple noncancerous (benign) growths (polyps) in the colon as early as their teenage years.
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However, ductal adenocarcinoma is associated with several cancer predisposition syndromes, such as hereditary pancreatitis (PRSS1 mutations), familial atypical mole and multiple melanoma (CDKN2 mutations), Peutz-Jeghers syndrome and other hereditary non-polyposis colon carcinomas (STK11 and germline mismatch repair genes), and syndromes associated with DNA repair gene mutations (such as BRCA2 and ATM).
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