A late diagnosis of MEN 1 Syndrome in a young patient initially pre-senting with nephrolithiasis
Multiple Endocrine Neoplasms Type 1 (MEN 1), originally called Wermer Syndrome, is a rare hereditary condition caused by mutations in the MEN1 tumor suppressor gene. It is characterized by tumors of the parathyroid glands, the anterior pituitary gland and pan-creatic islet cells. Hyperparathyroidism...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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Hrvatski liječnički zbor
2023-01-01
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| Series: | Liječnički vjesnik |
| Subjects: | |
| Online Access: | https://hrcak.srce.hr/file/453736 |