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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Bibliografische gegevens
Gepubliceerd in:Surg Case Rep
Hoofdauteurs: Shibata, Masahiro, Inaishi, Takahiro, Miyajima, Noriyuki, Adachi, Yayoi, Takano, Yuko, Nakanishi, Kenichi, Takeuchi, Dai, Noda, Sumiyo, Aita, Yuichi, Takekoshi, Kazuhiro, Kodera, Yasuhiro, Kikumori, Toyone
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Springer Berlin Heidelberg 2017
Onderwerpen:
Case Report
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5745210/
https://ncbi.nlm.nih.gov/pubmed/29282558
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40792-017-0408-x
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