Article
The eye in von Hippel-Lindau disease. Long-term follow-up of screening and treatment: recommendations.
Journal of internal medicine - 1 Jun 1998
Wittebol-Post D, Hes F J, Lips C J
Abstract excerpt
Von Hippel-Lindau disease (VHL) is an autosomal dominant tumour syndrome caused by germline mutations of the VHL tumour suppressor gene located on chromosome 3p25-26. In VHL tumours may occur in 14 different target organs, including the eye. Retinal angiomas are considered the first manifestation...
Topics
- Adult
- Female
- Follow-Up Studies
- Genetic Testing
- Genotype
- Hemangioma
- Humans
- Male
- Pedigree
- Phenotype
- Retinal Neoplasms
- Vision Screening
- von Hippel-Lindau Disease
