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Retinal function in the von Hippel-Lindau disease

✍ Scribed by Wojciech Lubiński; Karol Krzystolik; Cezary Cybulski; Zbigniew Szych; Krzysztof Penkala; Olgierd Palacz; Jan Lubiński

Book ID: 110428728
Publisher: Springer-Verlag
Year: 2003
Tongue: English
Weight: 169 KB
Volume: 106
Category: Article
ISSN: 0012-4486
DOI: 10.1023/a:1022919631288

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## Abstract Von Hippel‐Lindau (VHL) disease is an uncommon, autosomal dominant hereditary multitumor syndrome caused by germline alterations of the __VHL__ gene, which has been cloned recently and identified as a tumor suppressor gene. The major lesions in VHL disease include hemangioblastomas in t