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Knowing your patients’ cancer family history saves lives

With genomic technology advancing rapidly, we are quickly progressing into an exciting era where we will be able to practice truly personalized medicine and tailor patient care based on individual risk. To illustrate, every woman fits into one of 3 risk categories for breast cancer: those that carry sporadic, familial, or hereditary cancer risk. As the de facto primary care providers for many women, we have the responsibility to stratify every patient into one of these 3 categories in order to properly adapt screening and management decisions. Additionally, a focus on family history and risk stratification allows us the opportunity to detect those patients who carry one of several genetic mutations that dramatically increase their risk of developing cancer.

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This supplement is sponsored by Myriad Genetic Laboratories.
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Adam A. Ofer, MD

Director of Gynecology, Norwalk Hospital, Norwalk, Connecticut

Dr. Ofer reports that he is a speaker for Myriad Genetic Laboratories

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Adam A. Ofer, MD

Director of Gynecology, Norwalk Hospital, Norwalk, Connecticut

Dr. Ofer reports that he is a speaker for Myriad Genetic Laboratories

Author and Disclosure Information

 

Adam A. Ofer, MD

Director of Gynecology, Norwalk Hospital, Norwalk, Connecticut

Dr. Ofer reports that he is a speaker for Myriad Genetic Laboratories

Article PDF
Article PDF
Sponsor
This supplement is sponsored by Myriad Genetic Laboratories.
Sponsor
This supplement is sponsored by Myriad Genetic Laboratories.

With genomic technology advancing rapidly, we are quickly progressing into an exciting era where we will be able to practice truly personalized medicine and tailor patient care based on individual risk. To illustrate, every woman fits into one of 3 risk categories for breast cancer: those that carry sporadic, familial, or hereditary cancer risk. As the de facto primary care providers for many women, we have the responsibility to stratify every patient into one of these 3 categories in order to properly adapt screening and management decisions. Additionally, a focus on family history and risk stratification allows us the opportunity to detect those patients who carry one of several genetic mutations that dramatically increase their risk of developing cancer.

With genomic technology advancing rapidly, we are quickly progressing into an exciting era where we will be able to practice truly personalized medicine and tailor patient care based on individual risk. To illustrate, every woman fits into one of 3 risk categories for breast cancer: those that carry sporadic, familial, or hereditary cancer risk. As the de facto primary care providers for many women, we have the responsibility to stratify every patient into one of these 3 categories in order to properly adapt screening and management decisions. Additionally, a focus on family history and risk stratification allows us the opportunity to detect those patients who carry one of several genetic mutations that dramatically increase their risk of developing cancer.

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Knowing your patients’ cancer family history saves lives
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