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...

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Vydáno v:Endocr Pathol
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: 2017
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Article
On-line přístup: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
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