Natural History and Management of Familial Paraganglioma Syndrome Type 1: Long-Term Data from a Large Family

Head and neck paragangliomas are the most common clinical features of familial paraganglioma syndrome type 1 caused by succinate dehydrogenase complex subunit D (SDHD) mutation. The clinical management of this syndrome is still unclear. In this study we propose a diagnostic algorithm for SDHD mutati...

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Autors principals: Giulia Puliani, Franz Sesti, Tiziana Feola, Nicola Di Leo, Giorgia Polti, Monica Verrico, Roberta Modica, Annamaria Colao, Andrea Lenzi, Andrea M. Isidori, Vito Cantisani, Elisa Giannetta, Antongiulio Faggiano
Format: Artigo
Idioma:Inglês
Publicat: MDPI AG 2020-02-01
Col·lecció:Journal of Clinical Medicine
Matèries:
familial paraganglioma syndrome type 1
sdhd
paraganglioma
neuroendocrine neoplasm
Accés en línia:https://www.mdpi.com/2077-0383/9/2/588
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