Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis
نویسندگان
چکیده
منابع مشابه
MUTYH- Associated Polyposis
Lynch syndrome and familial adenomatous polyposis (FAP) have long been identifi ed as hereditary predisposition syndromes to colorectal cancer (CRC), most easily recognized on the basis of their autosomal dominant inheritance, young age of onset of CRC and other associated malignancies, and, in the case of FAP, the presence of adenomatous polyposis. However, in 2002 the fi rst report of a novel...
متن کاملMUTYH Associated Polyposis (MAP)
MUTYH Associated Polyposis (MAP), a Polyposis predisposition caused by biallelic mutations in the Base Excision Repair (BER) gene MUTYH, confers a marked risk of colorectal cancer (CRC). The MAP phenotype is difficult to distinguish from other hereditary CRC syndromes. Especially from Familial Adenomatous Polyposis (FAP) and to a lesser extend Lynch Syndrome, which are caused by germline mutati...
متن کاملBest practice guidelines for molecular analysis of colorectal polyposis: familial adenomatous polyposis coli (FAP) and MUTYH-associated polyposis (MAP)
Background:. UK Clinical Molecular Genetics Society (CMGS) consensus best practice guidelines for molecular analysis of familial adenomatous polyposis coli (FAP) were published in 2000. Technological developments in molecular testing for FAP together with the clinical and molecular characterisation of MUTYH-associated polyposis (MAP) led to the need to update the original FAP guidelines which w...
متن کاملThe polypoid ganglioneuroma associated with hyperplastic polyposis
Ganglioneuroma (GN) of the gastroin-testinal (GI) tract is rare tumor composed of ganglion cells, nerve fibers, and supporting cells of the enteric nervous system. Diffuse ganglioneuromatosis is associated with multiple endocrine neoplasia IIB (MEN IIB), neurofibro-matosis type I (NF1, also known as von Recklinghausen disease), multiple cu-taneous or GI tract neurofibromatosis, and neurogenic s...
متن کاملControlling the disease in MYH-associated polyposis
Background MYH-Associated Polyposis (MAP) is an autosomal recessive condition caused by bi-allelic mutations in MYH. Individuals with MAP tend to develop numerous polyps in their colon and rectum and have an increased risk of developing colorectal cancer. Recommendations for MAP treatment vary in the literature ranging from frequent surveillance colonoscopy to prophylactic surgery depending on ...
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ژورنال
عنوان ژورنال: Frontiers in Immunology
سال: 2018
ISSN: 1664-3224
DOI: 10.3389/fimmu.2018.00918