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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Bibliografiske detaljer
Udgivet i:J Endocr Soc
Main Authors: LaChance, David, Hoang, Thanh Duc, Shakir, Mohamed K M
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2020
Fag:
Neuroendocrinology and Pituitary
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208518/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.090
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