<p>Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors that arise from chromaffin cells in the adrenal medulla and in extra-adrenal locations, respectively. PPGL has the strongest hereditary risk of all endocrine neoplasms with about 40% of cases harboring germline mutations and another 25-30% of cases arising from somatic mutations. To date, over 20 susceptibility genes have been suggested to play a role in PPGL pathogenesis, with more genes still being researched. This project will seek to identify new candidate genes in apparently sporadic PPGLs to reveal a possible genetic background in cases without variants in known susceptibility genes. Knowledge of the genetic background and the genes involved in the pathogenesis of PPGL allows for clustering and/or development of targeted therapies for the tumors that cannot be surgically resected or tumors that have metastasized.</p>

Gene Variants in Pheochromocytoma and Paraganglioma

1 selected publication including "Germline SUCLG2 Variants in Patients with Pheochromocytoma and Paragan..." (29 citations)

Gene Variants in Pheochromocytoma and Paraganglioma

Germline SUCLG2 Variants in Patients with Pheochromocytoma and Paraganglioma.