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Article

Von Hippel-Lindau (VHL) disease: an update on the clinico-pathologic and genetic aspects.

Advances in anatomic pathology - 1 May 2008

Shehata Bahig M, Stockwell Christina A, Castellano-Sanchez Amilcar A, Setzer Shannon, Schmotzer Christine L, Robinson Haynes

Abstract excerpt

von Hippel-Lindau (VHL) disease is an inherited multisystem familial cancer syndrome caused by mutations of the VHL gene on chromosome 3p25. A wide variety of neoplastic processes are known to be associated with VHL disease. The consequences of the VHL mutations and the pathway for tumor development continue to be elucidated. This paper will detail the variety of tumors associated with VHL disease and discuss the...

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Source

Identifiers

PMID: 18434768
DOI: 10.1097/PAP.0b013e31816f852e

Genes

VHL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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