Von Hippel-Lindau Disease and Pheochromocytoma

J Gordon Millichap

doi:10.15844/pedneurbriefs-7-12-3

Von Hippel-Lindau Disease and Pheochromocytoma

Pediatric Neurology Briefs

Volume 7 (1993): Issue 12

By: J Gordon Millichap

Open Access

|Dec 1993

Abstract

Nineteen percent of 82 unselected patients with pheochromocytoma studied at the University of Freiburg, Germany, and the University of California, San Diego, were found to be gene carriers of von Hippel-Lindau disease.

References

Neumann HPH Berger DP Sigmund G Blum U Schmidt D Parmer RJ Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease N Engl J Med 1993 Nov 18 329 21 1531 1538 10.1056/NEJM199311183292103 8105382
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Tisherman SE Tisherman BG Tisherman SA Dunmire S Levey GS Mulvihill JJ Three-decade investigation of familial pheochromocytoma. An allele of von Hippel-Lindau disease? Arch Intern Med 1993 Nov 22 153 22 2550 2556 10.1001/archinte.1993.00410220046005 8239848
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-7-12-3 | Journal eISSN: 2166-6482

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Language: English

Page range: 90 - 91

Published on: Dec 1, 1993

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Von Hippel-Lindau Disease,

Pheochromocytoma,

Hemangioblastoma

© 1993 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 7 (1993): Issue 12