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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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| Publicat a: | J Clin Endocrinol Metab |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Endocrine Society
2018
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| Matèries: | |
| Accés en línia: | 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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