Synchronous bilateral pheochromocytomas and paraganglioma with novel germline mutation in MAX: a case report

BACKGROUND: Recent advance of genetic testing has contributed to the diagnosis of hereditary pheochromocytoma and paraganglioma (PPGL). The clinical characteristics of hereditary PPGL are varying among the types of mutational genes. It is still difficult to specify the pathognomonic symptoms in the...

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Detalles Bibliográficos
Autores principales: Shibata, Masahiro, Inaishi, Takahiro, Miyajima, Noriyuki, Adachi, Yayoi, Takano, Yuko, Nakanishi, Kenichi, Takeuchi, Dai, Noda, Sumiyo, Aita, Yuichi, Takekoshi, Kazuhiro, Kodera, Yasuhiro, Kikumori, Toyone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745210/
https://www.ncbi.nlm.nih.gov/pubmed/29282558
http://dx.doi.org/10.1186/s40792-017-0408-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745210/
https://www.ncbi.nlm.nih.gov/pubmed/29282558
http://dx.doi.org/10.1186/s40792-017-0408-x

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