|Hereditary Paraganglioma-Pheochromocytoma Syndromes Panel
PHEO and PGL Associated Syndrome Panel | Hereditary Paraganglioma-Pheochromocytoma Syndromes Panel (3 Genes) | PHEO/PGL Syndrome | PGL/PCC | Hereditary Paraganglioma-Pheochromocytoma Syndrome
||Confirmation of Clinical Diagnosis
Panel includes SDHB, SDHC, & SDHD Sequence Analysis.|
Sequence Analysis for the three genes in the Hereditary Paraganglioma-Pheochromocytoma Syndromes Panel can be ordered separately, SDHB (#3185), SDHC (#3190), & SDHD (#3195).
Sequence Analysis is also available for Hereditary Paraganglioma-Pheochromocytoma Syndromes genes: SDHAF2 (#3230) and MAX (#9090). These genes are not part of this panel.
* Previously listed as test code 93600.
||Sequence analysis is performed in both forward and reverse directions
||SDHB, SDHC, SDHD
||Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, Succinate dehydrogenase cytochrome b560 subunit, Succinate dehydrogenase [ubiquinone] cytochrome b small subunit