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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Bibliografiset tiedot
Julkaisussa:J Endocr Soc
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2020
Aiheet:
Tumor Biology
Linkit: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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