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Revised 3132009 IRB 097092 Hereditary Cancer Risk Program W.H. and Peggy Smith BaylorSammons Breast Center Baylor University Medical Center at Dallas Family History and Risk Assessment Questionnaire
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How to fill out hereditary cancer risk program

How to fill out hereditary cancer risk program:
01
Begin by gathering all necessary personal and family medical history related to cancer. This includes information about any relatives who have been diagnosed with cancer, the type of cancer they had, their age at diagnosis, and any known genetic mutations within the family.
02
Find the hereditary cancer risk program form or questionnaire provided by your healthcare provider or genetic counselor. This form usually asks for detailed information about your personal and family history of cancer.
03
Fill out all sections of the form accurately and completely. Provide as much detail as possible, including the names and ages of relatives who had cancer, the specific types of cancer they had, whether they were diagnosed before or after the age of 50, and any other pertinent information.
04
If you have difficulty remembering or accessing certain information, reach out to family members or consult medical records to ensure accuracy.
05
Don't be afraid to ask for help or clarification if you encounter any confusing questions or terminology on the form. Your healthcare provider or genetic counselor is available to assist you throughout the process.
06
Once you have completed the form, make sure to review it for any errors or omissions. Double-check all information to ensure its accuracy.
07
Submit the filled-out hereditary cancer risk program form to your healthcare provider or genetic counselor as instructed. They will review the information and determine if you meet the criteria for genetic testing or further evaluation.
08
After submitting the form, follow any additional instructions given by your healthcare provider or genetic counselor, such as scheduling an appointment or undergoing genetic counseling, if necessary.
Who needs hereditary cancer risk program:
01
Individuals who have a personal history of cancer, especially if diagnosed at a young age.
02
Individuals with a known family history of certain types of cancer, such as breast, ovarian, colorectal, pancreatic, or prostate cancer.
03
People who have multiple family members on the same side of the family with a history of cancer.
04
Those with a family history of rare types of cancer or specific genetic mutations associated with an increased risk of cancer.
05
Individuals who want to better understand their inherited risk of developing cancer and make informed decisions about preventive measures such as increased screening or genetic testing.
06
People who are considering starting a family and want to assess the potential risk of passing on genetic mutations associated with cancer.
It is important to consult with a healthcare provider or genetic counselor to determine if you or your family would benefit from a hereditary cancer risk program and to receive appropriate guidance and support.
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What is hereditary cancer risk program?
The hereditary cancer risk program is a program aimed at identifying individuals who may have an increased risk of developing cancer due to genetic factors.
Who is required to file hereditary cancer risk program?
Healthcare providers and organizations are required to file the hereditary cancer risk program for their patients or members.
How to fill out hereditary cancer risk program?
The hereditary cancer risk program can be filled out by collecting relevant information about the individual's family history of cancer and genetic testing results, if available.
What is the purpose of hereditary cancer risk program?
The purpose of the hereditary cancer risk program is to assess an individual's risk of developing cancer based on their genetic profile and family history, and to provide appropriate prevention and early detection measures.
What information must be reported on hereditary cancer risk program?
The hereditary cancer risk program must include information about the individual's family history of cancer, genetic testing results, and any relevant medical history.
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