MEN4, the MEN1 Mimicker: A Case Series of three Phenotypically Heterogenous Patients With Unique CDKN1B Mutations

CONTEXT: Germline CDKN1B pathogenic variants result in multiple endocrine neoplasia type 4 (MEN4), an autosomal dominant hereditary tumor syndrome variably associated with primary hyperparathyroidism, pituitary adenoma, and duodenopancreatic neuroendocrine tumors. OBJECTIVE: To report the phenotype...

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Detalles Bibliográficos
Autores principales: Seabrook, Amanda, Wijewardene, Ayanthi, De Sousa, Sunita, Wong, Tang, Sheriff, Nisa, Gill, Anthony J, Iyer, Rakesh, Field, Michael, Luxford, Catherine, Clifton-Bligh, Roderick, McCormack, Ann, Tucker, Katherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Clinical Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282358/
https://www.ncbi.nlm.nih.gov/pubmed/35323929
http://dx.doi.org/10.1210/clinem/dgac162

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282358/
https://www.ncbi.nlm.nih.gov/pubmed/35323929
http://dx.doi.org/10.1210/clinem/dgac162

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