Abstract von Hippel–Lindau (VHL) disease is an inheritable condition with an incidence of 1
in 36 000 live births. Individuals with VHL develop benign and malignant tumors including …

Von Hippel-Lindau disease (VHL) is one of the most common inherited neoplasia
syndromes and is characterized by highly vascular tumors of the eyes, brain, and spine, as …

Abstract von Hippel Lindau disease (vHL) is caused by a hereditary predisposition to
multiple neoplasms, especially hemangioblastomas in the retina and CNS, renal cell …

As the understanding of the genetic etiology of childhood cancers increases, the need for
the involvement of experts familiar with the provision of genetic counseling for this …

The present third edition of the clinical guideline is the result of a thorough revision. The
diagnostic criteria have been changed: There is no longer a distinction between major and …

Abstract The Von Hippel–Lindau (VHL) disease is an autosomal dominant disorder
characterized by the predisposition for multiple tumors caused by germline mutations in the …

Abstract Background: Von Hippel–Lindau Disease (VHL) is an autosomal dominant
inherited systemic cancer syndrome that gives rise to cystic and highly vascularized tumors …

The autosomal dominant von Hippel‐Lindau disease (vHL) is associated with a lifelong risk
of tumor development, especially retinal and CNS hemangioblastomas, pheochromocytoma …

Purpose To develop guidelines for ocular surveillance and early intervention for individuals
with von Hippel-Lindau (VHL) disease. Design Systematic review of the literature …

Objective: Pheochromocytomas are a hallmark feature of von Hippel-Lindau disease (vHL).
To our knowledge, this is the first systematic review with meta-analysis evaluating the …