First Report of Bilateral Pheochromocytoma in the Clinical Spectrum of HIF2A-Related Polycythemia-Paraganglioma Syndrome

CONTEXT: Molecular genetic research has so far resulted in the identification of 10 well-characterized susceptibility genes for hereditary pheochromocytoma (PHEO) or paraganglioma (PGL). Recently, a new syndrome characterized by multiple PGLs and somatostatinomas associated with congenital polycythe...

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Bibliographische Detailangaben
Hauptverfasser: Taïeb, David, Yang, Chunzhang, Delenne, Blandine, Zhuang, Zhengping, Barlier, Anne, Sebag, Fréderic, Pacak, Karel
Format: Artigo
Sprache:Inglês
Veröffentlicht: Endocrine Society 2013
Schlagworte:
JCEM Online: Advances in Genetics
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3644612/
https://ncbi.nlm.nih.gov/pubmed/23539726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2013-1217
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