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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:J Endocr Soc
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Oxford University Press 2020
विषय:
Tumor Biology
ऑनलाइन पहुंच: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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