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An unusual phenotype of MEN1 syndrome with a SI-NEN associated with a deletion of the MEN1 gene

We report about a young female who developed an unusual and an aggressive phenotype of the MEN1 syndrome characterized by the development of a pHPT, malignant non-functioning pancreatic and duodenal neuroendocrine neoplasias, a pituitary adenoma, a non-functioning adrenal adenoma and also a malignan...

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Detalles Bibliográficos
Autores principales: Manoharan, Jerena, Lopez, Caroline L, Hackmann, Karl, Albers, Max B, Pehl, Anika, Kann, Peter H, Slater, Emily P, Schröck, Evelin, Bartsch, Detlef K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828980/
https://www.ncbi.nlm.nih.gov/pubmed/27076911
http://dx.doi.org/10.1530/EDM-16-0011