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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Bibliografski detalji
Izdano u:Surg Case Rep
Glavni autori: Shibata, Masahiro, Inaishi, Takahiro, Miyajima, Noriyuki, Adachi, Yayoi, Takano, Yuko, Nakanishi, Kenichi, Takeuchi, Dai, Noda, Sumiyo, Aita, Yuichi, Takekoshi, Kazuhiro, Kodera, Yasuhiro, Kikumori, Toyone
Format: Artigo
Jezik:Inglês
Izdano: Springer Berlin Heidelberg 2017
Teme:
Case Report
Online pristup: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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