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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Detalles Bibliográficos
Autores principales: Parisien-La Salle, Stefanie, Dumas, Nadine, Rondeau, Geneviève, Latour, Mathieu, Bourdeau, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736565/
https://www.ncbi.nlm.nih.gov/pubmed/31551924
http://dx.doi.org/10.3389/fendo.2019.00546

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736565/
https://www.ncbi.nlm.nih.gov/pubmed/31551924
http://dx.doi.org/10.3389/fendo.2019.00546

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