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Translational Medicine / 转化医学Pheochromocytoma, Genetic Syndromes

Karel Pacak

MD, PhD, DSc

🏢National Institutes of Health🌐USA

Senior Investigator and Section Chief

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Key Contributions

👥Biography 个人简介

Karel Pacak at the NIH is a world leader in the genetics and biology of pheochromocytoma and paraganglioma, having made landmark contributions to understanding hereditary susceptibility genes including SDHB, SDHD, and their clinical implications. His research has contributed to the recognition that over 30% of pheochromocytomas and paragangliomas are hereditary, transforming genetic testing recommendations. He has developed biochemical testing algorithms and imaging strategies optimized for each genetic subgroup. His work on the metabolic vulnerabilities of SDH-mutant tumors has contributed to therapeutic strategies.

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🧪Research Fields 研究领域

pheochromocytoma paraganglioma genetics
SDH mutations pheochromocytoma
MIBG therapy paraganglioma
hereditary pheochromocytoma syndromes
catecholamine biochemistry

🎓Key Contributions 主要贡献

Representative Works 代表性著作

📄Data Sources 数据来源

Last updated: 2026-04-01 | All information from publicly available academic sources

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