MON-918 Familial Paraganglioma: Familiar Case Report

Introduction: Pheochromocytomas and Paragangliomas (PGL) are rare tumors originating from chromaffin cells. They may be sporadic or associated with familial inherited genetic syndromes around 50-80%. There are several PGL syndromes, the most common being PGL 1 (SDHD mutations), PGL 2 (SDHAF), PGL 3...

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Detalles Bibliográficos
Publicado en:J Endocr Soc
Main Authors: Ricardo, Gustavo Piech, Naldi, Murilo Marques, Calasans, Camila Ricci, Chang, Claudia Veiga, Tirapeli, Renata da Cunha Scalco, Bueno, Cristina Bellotti Formiga, Scalissi, Nilza, Lima, Jose Viana
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2020
Assuntos:
Tumor Biology
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7209027/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.1150
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