A Unique Case of Metastatic, Functional, Hereditary Paraganglioma Associated With anSDHC Germline Mutation

CONTEXT: Mutations in genes encoding for the succinate dehydrogenase (SDH) complex are linked to hereditary paraganglioma syndromes. Paraganglioma syndrome 3 is associated with mutations inSDHC and typically manifests as benign, nonfunctional head and neck paragangliomas. DESIGN: We describe a case...

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Detalhes bibliográficos
Publicado no:J Clin Endocrinol Metab
Main Authors: Ong, Raquel Kristin S, Flores, Shahida K, Reddick, Robert L, Dahia, Patricia L M, Shawa, Hassan
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2018
Assuntos:
Case Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7263789/
https://ncbi.nlm.nih.gov/pubmed/29878124
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2017-01302
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