| Literature DB >> 25158662 |
Abstract
Cowden syndrome (CS) is a genetic disorder characterized by multiple benign tissue growths (i.e., hamartomas) and an increased risk of developing specific cancers, such as breast, thyroid, kidney, endometrial, or colorectal cancer (Genetics Home Reference, 2012). This genetic syndrome was named after a person diagnosed with the disorder (Lloyd & Dennis, 1963). CS is part of a larger syndrome called PTEN hamartomatous syndrome, which also includes Bannayan-Riley-Ruvalcaba syndrome, PTEN-related Proteus syndrome, and Proteus-like syndrome (Eng, 2014).Entities:
Keywords: Cowden syndrome; breast cancer; cancer prevention; genetic cancer syndromes; risk management
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Year: 2014 PMID: 25158662 DOI: 10.1188/14.ONF.555-557
Source DB: PubMed Journal: Oncol Nurs Forum ISSN: 0190-535X Impact factor: 2.172