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      Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma.

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          Abstract

          Families with von Hippel-Lindau disease have variable risk of pheochromocytoma. Patients with von Hippel-Lindau disease and pheochromocytoma identified by screening can have no characteristic signs or symptoms. Families with von Hippel-Lindau disease were screened and followed to describe the natural history of von Hippel-Lindau pheochromocytoma, and to correlate these findings with von Hippel-Lindau germline mutation.

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          Author and article information

          Journal
          J. Urol.
          The Journal of urology
          0022-5347
          0022-5347
          Sep 1999
          : 162
          : 3 Pt 1
          Affiliations
          [1 ] Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
          Article
          10.1097/00005392-199909010-00004
          10458336
          d5e2e688-f394-4b5f-8b2e-cbe15734da84
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