Pathological and genetic characterization of bilateral adrenomedullary hyperplasia in a patient with germline MAX mutation

BACKGROUND: In recent years, familial pheochromocytoma (PHEO) with germline mutations in the MAX (MYC Associated Factor X) gene has been reported in a few cases. Here we investigated a 25 years old patient with multiple PHEOs associated with a non-sense germline MAX mutation. Preoperative (18)F-FDOP...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Endocr Pathol
Autors principals: Romanet, Pauline, Guerin, Carole, Pedini, Pascal, Essamet, Wassim, Castinetti, Frédéric, Sebag, Fréderic, Roche, Philippe, Cascon, Alberto, Tischler, Arthur S., Pacak, Karel, Barlier, Anne, Taïeb, David
Format: Artigo
Idioma:Inglês
Publicat: 2017
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6287616/
https://ncbi.nlm.nih.gov/pubmed/27838885
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12022-016-9460-5
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars