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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Detalhes bibliográficos
Publicado no:Surg Case Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2017
Assuntos:
Case Report
Acesso em linha: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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