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This review discusses the advancements in genetic evaluation and testing for hereditary forms of cancer with a focus on next-generation sequencing (NGS) technology. It highlights the benefits and limitations of NGS in hereditary cancer clinics, the role of genetic counselors, and the importance of informed consent and appropriate test selection in the genetic assessment of cancer susceptibility.
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Genetic evaluation and testing involve analyzing an individual's genetic material to identify genetic disorders, predispositions to certain diseases, and understanding inherited traits.
Individuals who are undergoing medical assessment, family history evaluations, or those in high-risk categories for genetic disorders are often required to file genetic evaluation and testing.
To fill out genetic evaluation and testing, individuals typically need to provide personal medical history, family health history, and consent for testing, along with any specific information requested by the healthcare provider.
The purpose of genetic evaluation and testing is to provide insights into an individual's genetic health, facilitate early intervention for genetic conditions, inform treatment options, and support family planning decisions.
Information reported on genetic evaluation and testing must include test results, genetic variants detected, interpretation of the variants, recommendations for follow-up, and any relevant personal or family health history.
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