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Acronym of the network: Roseau Rare Cancer family : Famille_KApplication redesignation of national reference networks for rare adult cancers, incorporating the organization of double reading of malignant
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Specify the treatments, medications, or surgeries the person has undergone or is currently undergoing.
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Li-Fraumeni Syndrome form is typically needed for individuals who have been diagnosed with or are suspected of having Li-Fraumeni Syndrome.
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The form helps to document their medical history, symptoms, and any treatments received, which can be useful for medical professionals in providing appropriate care and treatment.
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Li-Fraumeni Syndrome is a hereditary cancer predisposition syndrome that significantly increases the risk of various cancers, particularly in children and young adults. The 'form' typically refers to documentation required for genetic testing or clinical evaluation.
Individuals who are suspected of having Li-Fraumeni Syndrome, typically those with a family history of cancers associated with the syndrome, are required to file the form.
To fill out the Li-Fraumeni Syndrome form, individuals should provide personal details such as name, contact information, family health history, and any previous diagnoses of cancer. It may also require consent for genetic testing.
The purpose of the Li-Fraumeni Syndrome form is to assess the risk of the syndrome in individuals, facilitate genetic testing, and gather necessary information for clinical evaluation and counseling.
Information required typically includes personal and family medical history, types of cancers in the family, ages at diagnosis, genetic testing results if available, and any current health issues.
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