MON-249 SDHD Mutation: Nonfunctional Paragangliomas Presenting as Bilateral Carotid Body Tumors with Syncope

SDHD Mutation: Nonfunctional paragangliomas presenting as bilateral carotid body tumors with syncope Background: A mutation of the SDHD gene is associated with hereditary paraganglioma-pheochromocytoma (PGL/PCC) syndromes which most commonly originate in the head and neck region, and usually form in...

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Detalles Bibliográficos
Autores principales: LaChance, David, Hoang, Thanh Duc, Shakir, Mohamed K M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Neuroendocrinology and Pituitary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208518/
http://dx.doi.org/10.1210/jendso/bvaa046.090

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208518/
http://dx.doi.org/10.1210/jendso/bvaa046.090

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