Multiple endocrine neoplasia type 1 familial case in a patient with insulinoma and primary hyperparathyroidism: First report in literature and in the Costa Rican population of the c.1224_1225insGTCC pathogenic variant

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder without a good genotype–phenotype correlation, characterized by tumor predisposition in the parathyroid gland, anterior pituitary, and pancreatic islet cells. Here, we describe a 37‐year‐old male with previous history o...

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Detalles Bibliográficos
Autores principales: Molina‐Céspedes, Paula, Ruiz‐Golcher, Ernesto José, Badilla‐Barboza, Oscar, Sedó‐Mejía, Giovanni, Barboza‐Rodríguez, Laura, Badilla‐Porras, Ramsés
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9994136/
https://www.ncbi.nlm.nih.gov/pubmed/36911651
http://dx.doi.org/10.1002/ccr3.7041

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9994136/
https://www.ncbi.nlm.nih.gov/pubmed/36911651
http://dx.doi.org/10.1002/ccr3.7041

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