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
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| Test Information: |
Confirmation of Clinical Diagnosis |
| Test Details |
| Test Code: |
3600 |
| Test Includes: |
Panel includes SDHB, SDHC, & SDHD Sequence Analysis.
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| Special Notes: |
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.
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| Technical Information |
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| Methodology: |
Sequence analysis is performed in both forward and reverse directions |
| Gene Name: |
SDHB, SDHC, SDHD |
| Protein Name: |
Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, Succinate dehydrogenase cytochrome b560 subunit, Succinate dehydrogenase [ubiquinone] cytochrome b small subunit |
