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Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports

Crossref DOI link: https://doi.org/10.1186/s13256-021-02852-z

Published Online: 2021-05-22

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Hirose, Rei

Tsurutani, Yuya https://orcid.org/0000-0001-5831-3286
Sugisawa, Chiho

Inoue, Kosuke

Suematsu, Sachiko

Nagata, Maki

Hasegawa, Naoki

Kakuta, Yukio

Yonamine, Masato

Takekoshi, Kazuhiro

Kimura, Noriko

Saito, Jun

Nishikawa, Tetsuo
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Article History

Received: 14 December 2020

Accepted: 5 April 2021

First Online: 22 May 2021

Declarations

:

: This study was conducted in accordance with the fundamental principles of the Declaration of Helsinki. Written informed consent was obtained from “patient 1” and the wife of “patient 2” before submission.

: Written informed consent was obtained from the patient and next of kin of the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

: The authors declare that they have no competing interests.

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