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First report of bilateral pheochromocytoma in the (...)

J Clin Endocrinol Metab. 2013 May ;98(5):E908-13
First report of bilateral pheochromocytoma in the clinical spectrum of HIF2A-related polycythemia-paraganglioma syndrome.
Taieb D, Yang C, Delenne B, Zhuang Z, Barlier A, Sebag F, Pacak K.

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 polycythemia due to somatic mutations in HIF2A has been reported.

PubMed

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