Revisão Revisado por pares

Familial adenomatous polyposis

2000; Wiley; Volume: 18; Issue: 4 Linguagem: Inglês

10.1002/(sici)1098-2388(200006)18

ISSN

8756-0437

Autores

Geeta Lal, Steven Gallinger,

Tópico(s)

Helicobacter pylori-related gastroenterology studies

Resumo

Familial adenomatous polyposis (FAP) is a dominantly inherited familial cancer syndrome characterized by an increased predisposition to colorectal cancer and other benign and malignant extra-colonic lesions. FAP has been linked to germline mutations of the adenomatous polyposis coli (APC) gene that encodes a protein with 2,843 amino acids that has important functions in the regulation of cell growth. A genotype-phenotype correlation has also been observed between mutations in the APC gene and polyp phenotype. We review the clinical and genetic features of this disorder and provide information on the diagnostic approaches and treatment options available for this disease. Semin. Surg. Oncol. 18:314–323. © 2000 Wiley-Liss, Inc.

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