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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Номзүйн дэлгэрэнгүй

Үндсэн зохиолчид:	Paula Molina‐Céspedes, Ernesto José Ruiz‐Golcher, Oscar Badilla‐Barboza, Giovanni Sedó‐Mejía, Laura Barboza‐Rodríguez, Ramsés Badilla‐Porras
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	Wiley 2023-03-01
Цуврал:	Clinical Case Reports
Нөхцлүүд:	multiple endocrine neoplasia primary hyperparathyroidism insulinoma hypoglycemia nephrolithiasis familial
Онлайн хандалт:	https://doi.org/10.1002/ccr3.7041
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!