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Six case reports of NTHL1-associated tumor syndrome further support it as a multi-tumor predisposition syndrome
Authors:Chelsey B. Weatherill  Sarah A. Burke  Carolyn G. Haskins  Darcy K. Berry  Jeanne P. Homer  Michael J. Demeure  Sourat Darabi
Affiliation:1. Hoag Family Cancer Institute, Newport Beach, California, USA;2. Department of Individualized Cancer Management, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA
Abstract:NTHL1-associated tumor syndrome (NATS) is an autosomal recessive condition characterized by an increased risk for colorectal polyposis and colorectal cancer (CRC). Only 46 case reports have been previously published. In a retrospective review, we analyzed the clinical histories of six patients found to have NATS after genetic counseling and testing. NATS appears to be associated with an increased risk for colorectal polyposis, CRC, female breast cancer, meningiomas, and endometrial cancer. Although research is limited, prior publications have reported a multi-tumor predisposition for individuals with biallelic pathogenic or likely pathogenic variants in NTHL1. Additional data are necessary to further define the cancer risks so affected individuals can be appropriately managed.
Keywords:breast cancer  cancer genetics  colorectal cancer  genetic predisposition  hereditary  meningioma  NTHL1  NTHL1-associated tumor syndrome  polyposis
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