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Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients

4 Oct 2018

Abstract excerpt

Pheochromocytoma and paragangliomas (PCC/PGL) are neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla and sympathetic/parasympathetic ganglia, respectively. Of clinical relevance regarding diagnosis is the highly variable presentation of symptoms in PCC/PGL patients. To date, the clear-cut correlations between the genotypes and phenotypes of PCC/PGL have not been entirely established. In...

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PMID: 30352407
DOI: 10.1530/ec-18-0325

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