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- W2991384865 abstract "Hyperparathyroidism is present in up to 30% of patients with MEN2A and is associated with one of the high-risk mutations, codon 634. Patients at risk for MEN2A should undergo genetic testing, and patients with MEN2A should be biochemically screened for hyperparathyroidism before prophylactic or curative thyroidectomy. The surgical approach for hyperparathyroidism in MEN2A depends on the surgeon's discretion and the individual patient's clinical factors. Despite excellent short-term eucalcemia rates, given the high rate of multigland disease, MEN 2A patients with primary hyperparathyroidism should undergo lifelong surveillance for recurrence." @default.
- W2991384865 created "2019-12-05" @default.
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- W2991384865 date "2020-01-01" @default.
- W2991384865 modified "2023-10-17" @default.
- W2991384865 title "Advances in Diagnosis and Management of Primary Hyperparathyroidism due to Multiple Endocrine Neoplasia (MEN) Type 2 Syndrome" @default.
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- W2991384865 doi "https://doi.org/10.1016/b978-0-323-66195-9.00011-x" @default.
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