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Cancers can be hereditary; the key lies in genetic diagnosis.

Portfolio of genetic studies for the diagnosis of hereditary cancer.

It includes everything from a family variant to specific panels designed based on national and international clinical guidelines.

G-Essence Mama

It is indicated in patients where hereditary breast cancer is suspected due to personal and/or family history, where this is the only type of cancer detected.
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G-Essence Gynecomastia

indicates in those patients where hereditary cancer is suspected due to personal history.
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G-Essence Colon

It is recommended that this panel be indicated for patients with a personal and/or family history of hereditary prostate cancer, as it is the only type of cancer detected.
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G-Essence Prostate

It is recommended that this panel be indicated for patients with a personal and/or family history of hereditary prostate cancer, which is the only type of cancer detected.
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G-Essence Melanoma

This panel is recommended for patients with a personal and/or family history suggesting hereditary skin cancer, this being the only type of cancer detected.
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G-Essence BRCA 1 and 2 (Germinal)

It is indicated in patients with a personal and/or family history of suspected hereditary breast, ovarian, pancreatic, or prostate cancer. According to the guidelines, this study would be limited to cases in which the study is indicated.
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G-Essence 30

It is indicated in patients with a family and/or personal history of more than one type of cancer and suspected hereditary origin. E.g.: breast, colon, ovary, endometrium, pancreas, prostate.
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G-Essence 50

It is indicated in patients with a family and/or personal history of more than one type of cancer and suspected hereditary origin. E.g.: breast, colon, ovary, endometrium, pancreas, prostate.
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G-Essence 100

It is indicated in patients where hereditary cancer is suspected due to personal history (specific type of tumor, such as ovarian and pancreatic cancer) and/or family history.
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G-Essence Plus

It is indicated in patients where hereditary cancer is suspected due to personal history (specific type of tumor, such as ovarian and pancreatic cancer) and/or family history. It also includes the possibility of performing DPYD gene testing, as a pharmacogenomic study, which is essential for defining treatment in patients with colon or breast cancer who require capecitabine.
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Family variant

It is recommended for all patients belonging to a family with hereditary syndrome with a known mutation.
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