Phenotypes Associated With MEN1 Syndrome: A Focus on Genotype-Phenotype Correlations

Phenotypes Associated With MEN1 Syndrome: A Focus on Genotype-Phenotype Correlations

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited tumor syndrome, associated with parathyroid, pituitary, and gastro-entero-pancreatic (GEP) neuroendocrine tumors (NETs). MEN1 is usually consequent to different germline and somatic mutations of the MEN1 tumor suppress...

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Bibliographic Details
Main Authors: Chiara Mele, Monica Mencarelli, Marina Caputo, Stefania Mai, Loredana Pagano, Gianluca Aimaretti, Massimo Scacchi, Alberto Falchetti, Paolo Marzullo
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Endocrinology
Subjects:
MEN1
genotype
phenotype
mutations
tumors
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2020.591501/full

Internet

https://www.frontiersin.org/articles/10.3389/fendo.2020.591501/full

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