Isolated Pheochromocytoma in a 73-Year-Old Man With No Clinical Manifestations of Type 1 Neurofibromatosis Carrying an Unsuspected Deletion of the Entire NF1 Gene

Pheochromocytomas (PHEOs) are a rare cause of endocrine hypertension that requires genetic counseling since at least 30% of PHEOs are associated with a germline mutation in a susceptibility gene. Neurofibromatosis type 1, NF1 is amongst the 16 known causing genes for pheochromocytomas/paragangliomas...

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Autors principals:	Stefanie Parisien-La Salle, Nadine Dumas, Geneviève Rondeau, Mathieu Latour, Isabelle Bourdeau
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2019-08-01
Col·lecció:	Frontiers in Endocrinology
Matèries:	neurofibromatosis deletion phenotype pheochromocytoma hypertension
Accés en línia:	https://www.frontiersin.org/article/10.3389/fendo.2019.00546/full
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