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Get the free Referral for Hereditary Cancer Risk Assessment

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This document serves as a referral form for patients to assess hereditary cancer risks, allowing healthcare providers to indicate specific criteria relevant to cancer history and familial relationships.
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How to fill out referral for hereditary cancer

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How to fill out Referral for Hereditary Cancer Risk Assessment

01
Obtain the referral form from the healthcare provider or clinic.
02
Fill in the patient's demographic information, including name, date of birth, and contact details.
03
Provide the patient's medical history, including any past diagnoses of cancer and family history of cancer.
04
Indicate any known genetic mutations in the family, if applicable.
05
Include the reason for referral, specifying any concerning symptoms or family history.
06
Submit the completed referral form to the appropriate specialist or clinic for hereditary cancer risk assessment.

Who needs Referral for Hereditary Cancer Risk Assessment?

01
Individuals with a personal history of certain cancers, especially those diagnosed at a young age.
02
Family members of individuals with known hereditary cancer syndromes.
03
Patients with multiple relatives diagnosed with the same type of cancer.
04
People with specific ethnic backgrounds that have a higher prevalence of certain genetic mutations.
05
Individuals who have questions about their risk of hereditary cancer based on family history.
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What is MyRisk with RiskScore? MyRisk can help you and your provider understand your risk of developing 11 different types of cancer, including cancer. It can also provide important information for your family members if your test reveals a genetic change associated with hereditary cancer.
Hereditary cancer risk assessment (HCRA) is a multidisciplinary process of estimating probabilities of germline mutations in cancer susceptibility genes and assessing empiric risks of cancer, based on personal and family history.
An assessment includes information on personal and family history, including pathology, imaging reports, and evaluation of other medical risk factors for cancer.
A cancer risk assessment is a way to gather information about various cancer risk factors. It's used to help understand a person's individual risk for developing cancer. The goal of a cancer risk assessment is to help guide a person and their health care team when making decisions about their health and care.
You'll usually have an appointment with a genetic counsellor or specialist who will find out if you need genetic tests to check if you're at higher risk of getting certain cancers.
Genetic tests (DNA tests) can detect inherited (hereditary) genetic mutations that increase your cancer risk. Some of the most common mutations involve the P53 gene and the BRCA genes.
During genetic testing for cancer risk, a healthcare provider tests your body fluid (usually blood or saliva) for one or more of these hereditary mutations. But having a cancer-related mutation doesn't mean you will get cancer. It just means you're at increased risk.

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Referral for Hereditary Cancer Risk Assessment is a process by which individuals are evaluated for their genetic predisposition to certain hereditary cancers, allowing for risk management and early detection strategies.
Healthcare providers, such as doctors or genetic counselors, may file a referral for hereditary cancer risk assessment on behalf of patients who meet specific criteria indicating a higher risk for hereditary cancers.
To fill out the referral, the healthcare provider typically collects patient's personal and family medical history, including instances of cancer, relevant demographics, and any previous genetic testing results, and then documents this information in the designated referral form.
The purpose of the referral is to identify individuals who may benefit from genetic testing and to guide them toward appropriate risk-reducing strategies and surveillance for hereditary cancers.
Information that must be reported includes the patient's medical and family history, specific cancers within the family, the patient's age and demographics, and any prior genetic test results or concerns related to hereditary cancer risks.
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