Hereditary Pheochromocytoma and Paraganglioma Syndrome
| Test Information | |
|---|---|
| Test Name | Hereditary Pheochromocytoma and Paraganglioma Syndrome |
| Lab (Location) | University Health Network |
| Category | Cancer |
| Subcategory | Hereditary Pheochromocytoma and Paraganglioma |
| Test type | Gene Panel |
| Samples Accepted | Blood, DNA, Saliva |
| Indications Diagnosis | Diagnosis, Carrier / Cascade Testing |
| Test Methodology | CNV, Sequencing |
| Methodology Notes | FH, MAX, MEN1, NF1, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127, VHL |
| Diseases/Conditions | Pheochromocytoma, Paraganglioma, Von Hippel Lindau, Neurofibromatosis type I, Multiple Endocrine Neoplasia (Types 1 and 2) |