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Breast Cancer High Risk Extended Panel Plus Test Methodology Medical Diagnostic Laboratories, L.L.C. (MDL) is utilizing targeted next generation sequencing (NGS) technology to test germ line variants in
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To fill out breast cancer high risk, follow these steps:
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Gather all the necessary information, such as personal medical history, family medical history, and lifestyle habits.
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Consult with a healthcare professional, such as an oncologist or a genetic counselor, who can guide you through the process.
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Complete any required questionnaires or forms provided by the healthcare professional.
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Provide accurate and detailed information about any previous breast or ovarian cancer diagnoses in yourself or close relatives.
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Include information about any known genetic mutations that increase the risk of breast cancer, such as BRCA1 or BRCA2.
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Answer questions regarding lifestyle factors that may contribute to breast cancer risk, such as smoking, alcohol consumption, and hormone replacement therapy.
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Submit the completed breast cancer high risk form to the healthcare professional for further evaluation and recommendations.
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Follow any additional instructions or recommendations provided by the healthcare professional based on the assessment of your high-risk status.

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Breast cancer high risk assessments are typically recommended for individuals who:
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- Have a personal history of breast or ovarian cancer
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- Have a family history of breast or ovarian cancer, especially if the relatives diagnosed were close family members like parents, siblings, or children
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- Have a family history of known genetic mutations that increase the risk of breast cancer, such as BRCA1 or BRCA2
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- Have certain risk factors, such as early menstruation, late menopause, nulliparity (no history of childbirth), or a history of atypical hyperplasia or lobular carcinoma in situ
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- Have been exposed to factors or treatments that may increase the risk of breast cancer, such as radiation therapy to the chest at a young age
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- Have requested an assessment due to concerns about their individual risk of developing breast cancer
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Breast cancer high risk refers to individuals who have a significantly increased probability of developing breast cancer due to genetic, familial, or personal health factors.
Individuals who have been identified as having high risk factors for breast cancer, such as a family history of the disease or specific genetic mutations, are typically required to file for breast cancer high risk.
Filling out breast cancer high risk involves completing a specific form that usually requires personal information, medical history, family history of breast cancer, and any genetic testing results.
The purpose of identifying and filing for breast cancer high risk is to facilitate early detection, preventative measures, and targeted treatment options for individuals at increased risk.
The information that must be reported includes the individual's personal health details, family history of breast cancer, results from any genetic testing, and lifestyle factors that may contribute to the risk.
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