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Von-Hippel-Lindau-Syndrom

✍ Scribed by Reith, W.; Körner, H.


Book ID
121415175
Publisher
Springer
Year
2013
Tongue
German
Weight
333 KB
Volume
53
Category
Article
ISSN
0033-832X

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Von Hippel-Lindau (VHL) syndrome (OMIM 193300) is an autosomal dominant disorder caused by deletions or mutations in a tumor suppressor gene mapped to human chromosome 3p25. It is characterized clinically by vascular tumors, including retinal and central nervous system hemangioblastomas (cerebellar,