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Correspondence
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Volume 330:1090-1091 April 14, 1994 Number 15
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Pheochromocytoma, Multiple Endocrine Neoplasia Type 2, and von Hippel-Lindau Disease

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 by Neumann, H.
To the Editor: The report by Neumann et al. (Nov. 18 issue)1 underscores the importance of screening for hereditary disorders in patients with pheochromocytoma. The authors' determination, however, that 23 percent of unselected patients with pheochromocytoma had hereditary disease is a higher figure than that in any prior report, including one series not listed by the authors in which the figure was approximately 7 percent2. The authors may be correct, but there could be an ascertainment bias, a possibility they suggested in a previous article in which they reported a high incidence of von Hippel-Lindau syndrome in the Freiburg . . . [Full Text of this Article]

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