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Sex and the law
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Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed. Multiple endocrine neoplasia Type 1 MEN1 is a frequent form of MEN see this term , a rare inherited cancer syndrome, characterized by the development of neuroendocrine tumors of the parathyroid, pancreas, and anterior pituitary gland, and less commonly the adrenal cortical gland, with other non-endocrine tumors in some patients. The sex ratio in MEN1 appears to be equal. In individuals with MEN1, tumors can develop at any age. The most common initial manifestation is primary hyperparathyroidism from 20 years.
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