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The RET gene, or "rearranged during transfection" proto-oncogene, is a gene that can become a cancer-causing gene, or oncogene. Mutations in the RET gene are associated with hereditary disorders like medullary thyroid carcinoma and multiple endocrine neoplasia (MEN2).12

In medullary thyroid carcinoma, RET mutations lead to abnormally high levels of calcitonin, a hormone that regulates calcium in the blood. While calcitonin levels are elevated, patients do not experience low blood calcium because their tissues are resistant to the hormone.1

For individuals carrying a RET mutation, there is a high risk of developing medullary thyroid carcinoma, often at a young age. Consequently, a thyroidectomy (removal of the thyroid gland) is typically recommended early in life to prevent tumor development.1

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