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Published in 2020 at "Case Reports in Endocrinology"
DOI: 10.1155/2020/8824640
Abstract: Von Hippel–Lindau disease is an autosomal dominant inherited syndrome predisposing to a variety of highly vascularised tumors in different organs. Although bilateral pheochromocytoma was reported in patients with von Hippel–Lindau disease, the coexistence of primary…
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Keywords:
bilateral pheochromocytoma;
hippel lindau;
lindau disease;
von hippel ... See more keywords