An analysis of surveillance screening for SDHB-related disease in childhood and adolescence
Objective: Phaeochromocytomas (PCC) and paragangliomas (PGL) are rare in children. A large proportion of these are now understood to be due to underlying germline mutations. Here we focus on succinate dehydrogenase subunit B (SDHB) gene mutation carriers as these tumours carry a high risk of maligna...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Bioscientifica
2019-02-01
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Series: | Endocrine Connections |
Subjects: | |
Online Access: | https://ec.bioscientifica.com/view/journals/ec/8/3/EC-18-0522.xml |