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Comprehensive treatment of rare multiple endocrine neoplasia type 1: A case report
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare hereditary disorder caused by mutations of the MEN1 gene. It is characterized by hyperparathyroidism and involves the pancreas, anterior pituitary, duodenum, and adrenal gland. Here, we report a 40-year-old male patient with MEN1 who f...
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| Publicado no: | World J Clin Cases |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7322426/ https://ncbi.nlm.nih.gov/pubmed/32607345 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v8.i12.2647 |
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