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A Rare Presentation of Multiple Endocrine Neoplasia Type 1
Background: Multiple endocrine neoplasia type 1 (MEN1) is a rare, autosomal dominant inherited syndrome caused by mutations in the MEN1 tumor suppressor gene with a reported incidence of 2 in 100,000. Clinical Case: A 26-year-old Caucasian female was seen for surveillance screening given positive fa...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265614/ http://dx.doi.org/10.1210/jendso/bvab048.2022 |