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...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Bioscientifica
2019-02-01
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| Col·lecció: | Endocrine Connections |
| Matèries: | |
| Accés en línia: | https://ec.bioscientifica.com/view/journals/ec/8/3/EC-18-0522.xml |
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