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 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

Abstract 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...

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Bibliographic Details
Main Authors: Paula Molina‐Céspedes, Ernesto José Ruiz‐Golcher, Oscar Badilla‐Barboza, Giovanni Sedó‐Mejía, Laura Barboza‐Rodríguez, Ramsés Badilla‐Porras
Format: Article
Language:English
Published: Wiley 2023-03-01
Series:Clinical Case Reports
Subjects:
multiple endocrine neoplasia
primary hyperparathyroidism
insulinoma
hypoglycemia
nephrolithiasis
familial
Online Access:https://doi.org/10.1002/ccr3.7041
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