Medline ® Abstract for Reference 36
of 'Molecular biology and pathogenesis of von Hippel-Lindau disease'
von Hippel-Lindau disease.
Couch V, Lindor NM, Karnes PS, Michels VV
Mayo Clin Proc. 2000;75(3):265.
An autosomal dominant tumor predisposition syndrome, von Hippel-Lindau disease (VHL) is characterized by the presence of benign and malignant tumors. Hallmark lesions include retinal angiomas, hemangioblastomas of the cerebellum and spinal cord, and renal cell carcinomas. Affected persons may also have angiomatous or cystic lesions of the kidneys, pancreas, and epididymis, as well as adrenal pheochromocytomas. In this article, we discuss the clinical features and diagnostic criteria for this clinically underdiagnosed condition. An update on recent findings regarding the molecular genetics of VHL is provided, including a discussion of the evolving understanding of genotype-phenotype correlations. Understanding the molecular and functional aspects of this condition will lead to the development of strategies for the management and treatment of inherited and sporadic VHL-associated tumors.
Department of Medical Genetics, Mayo Clinic Rochester, Minn. 55905, USA.