Abstract | INTRODUCTION: CASE REPORT: CONCLUSION: The multitude of VHL-associated tumors and intra-familial variability in clinical expressivity render early diagnosis of VHL difficult. We therefore shortly illustrate the spectrum of clinical phenotypes and the VHL screening and surveillance guidelines.
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Authors | Markus Joerger, Dieter Koeberle, Hartmut P H Neumann, Silke Gillessen |
Journal | Onkologie
(Onkologie)
Vol. 28
Issue 3
Pg. 159-63
(Mar 2005)
ISSN: 0378-584X [Print] Switzerland |
PMID | 15772467
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't, Review)
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Topics |
- Adult
- Diagnosis, Differential
- Diagnostic Errors
(prevention & control)
- Female
- Humans
- Practice Guidelines as Topic
- Practice Patterns, Physicians'
- Rare Diseases
(diagnosis, therapy)
- von Hippel-Lindau Disease
(diagnosis, therapy)
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