The Clinical Phenotype of SDHC-Associated Hereditary Paraganglioma Syndrome (PGL3)

摘要

Context:Mutations in the genes encoding subunits of the succinate dehydrogenase complex cause hereditary paraganglioma syndromes. Although the phenotypes associated with the more commonly mutated genes, SDHB and SDHD, are well described, less is known about SDHC -associated paragangliomas.