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Familial Colorectal Cancer: Diagnosis, Genetics and Management Saturday, October 11, 2014, The Inn at St. Johns, Plymouth, MI UM DEPARTMENT OF INTERNAL MEDICINE CONTINUING MEDICAL EDUCATION www.med.umich.edu/intmed/cme
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How to fill out familial colorectal cancer:

01
Educate yourself: Familiarize yourself with the basics of familial colorectal cancer, including risk factors, screening and prevention methods, and available treatment options. This will help you understand the condition better and make informed decisions.
02
Understand your family history: It is crucial to gather information about your family's medical history, specifically related to colorectal cancer. Identify any patterns or instances of the disease among close relatives such as parents, siblings, and children.
03
Consult with a healthcare professional: Schedule an appointment with a healthcare professional, preferably a gastroenterologist or a genetic counselor, who specializes in familial colorectal cancer. They can assess your risk factors, evaluate your family history, and provide personalized recommendations.
04
Genetic testing: In some cases, your healthcare provider may recommend genetic testing to identify specific gene mutations associated with familial colorectal cancer. This can help determine if you carry any inherited mutations that increase your risk.
05
Discuss screening options: Based on your risk factors and family history, your healthcare provider will recommend an appropriate screening schedule. Common screening methods for familial colorectal cancer include colonoscopies, stool tests, and genetic markers.
06
Follow screening guidelines: Adhere to the recommended screening guidelines outlined by your healthcare provider. Regular screenings can help detect colorectal cancer early or even detect pre-cancerous polyps, increasing the chances of successful treatment.

Who needs familial colorectal cancer?

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Individuals with a family history: People with immediate family members (parents, siblings, or children) who have had colorectal cancer are at an increased risk and should consider familial colorectal cancer screening.
02
Those with a history of hereditary colorectal cancer syndromes: Certain hereditary syndromes, such as Lynch syndrome or familial adenomatous polyposis (FAP), significantly elevate the risk of developing colorectal cancer. Screening is crucial for individuals with a personal or family history of these syndromes.
03
People with a history of inflammatory bowel disease (IBD): Individuals diagnosed with conditions like ulcerative colitis or Crohn's disease are at a higher risk of developing colorectal cancer. Regular screenings are essential in these cases.
04
Individuals aged 50 and above: Although familial colorectal cancer primarily affects those with a family history, routine colorectal cancer screening is recommended for all individuals aged 50 and above, regardless of their family history, as age is a significant risk factor for developing the disease.
Remember, it is always best to consult with a healthcare professional who can assess your individual risk factors and provide personalized guidance on familial colorectal cancer screening and prevention.
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Familial colorectal cancer is a hereditary condition where multiple family members have been diagnosed with colorectal cancer.
Individuals with a family history of colorectal cancer are recommended to file familial colorectal cancer for early detection and prevention.
One can fill out familial colorectal cancer by providing detailed information about family history of colorectal cancer and undergoing screenings.
The purpose of familial colorectal cancer is to identify individuals at higher risk for colorectal cancer and take preventive measures.
Information such as family medical history, number of relatives diagnosed with colorectal cancer, and any genetic testing results need to be reported on familial colorectal cancer.
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