Transgender and gender diverse (TGD) populations with hereditary cancer syndromes face
unique obstacles to identifying and obtaining appropriate cancer surveillance and risk …

Approximately 24 million people in the United States identify as transgender, non-binary, or
gender-diverse, and they often face challenges in accessing health care related to …

INTRODUCTION: Transgender and gender diverse (TGD) populations with hereditary
cancer syndromes face unique barriers to care and thus may not be accessing appropriate …

Clinical guidelines recommend universal tumor screening (UTS) of colorectal and
endometrial cancers for Lynch syndrome (LS). There are limited guidelines for how to …

Simple Summary Lynch syndrome is the most common cause of hereditary colorectal
cancer, but is also associated with increased extracolonic cancer risk, including upper …

Objectives Lynch syndrome increases risks for colorectal and other cancers. Though
published Lynch syndrome cancer risk-management guidelines are effective for risk …

Identifying individuals who have Lynch syndrome involves a complex diagnostic workup that
includes taking a detailed family history and a combination of various tests such as …

BACKGROUND Lynch syndrome (LS) is a hereditary cancer predisposition syndrome
associated with increased risk of multiple cancers. While colorectal cancer surveillance …

PURPOSE Identification of those at risk of hereditary cancer syndromes using electronic
health record (EHR) data sources is important for clinical care, quality improvement, and …

Universal screening of all newly diagnosed colorectal cancer tumors can identify individuals
at high risk for Lynch syndrome (LS), a hereditary cancer syndrome predisposing carriers to …