Related Gene(s): FH, MAX, MEN1, NF1, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127, VHL
Next generation sequencing (NGS) is used to offer a comprehensive hereditary paraganglioma (PGL)/pheochromocytomas (PCC) panel. Genes on this panel include FH, MAX, MEN1, NF1, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127, and VHL. Full gene sequencing and gross deletion/duplication analysis is performed for all 12 genes. Specific Site Analysis is available for individual gene mutations identified in a family.
This test will be available soon. For additional information, please contact us.