ABSTRACT Background: von Hippel–Lindau (VHL) syndrome is a multisystem neoplastic
disorder involving eyes, central nervous system, kidneys, spine, and other tissues. A retinal …

Background: Von Hippel-Lindau syndrome is a rare autosomal dominantly inherited
multisystemic oncologic syndrome, presenting predominantly with angiomatosis in …

ABSTRACT Clinical case: A 35-year-old man with a family history of von Hippel-Lindau
disease was diagnosed to have two retinal hemangiomas in the right eye and another in the …

Retinal hemangioblastoma is associated with Von-Hippel–Lindau syndrome. Here, we
report the case of a 50-year-old man who had a retinal hemangioblastoma that penetrated …

BACKGROUND AND OBJECTIVE: To describe a case series of three patients in one family
with Von Hippel-Lindau (VHL) disease who presented with vitreoretinal neovascularization …

2. Discussion VHL is an autosomal dominant, multisystem, progressive cancer syndrome
caused by mutations of the VHL tumor suppressor gene, located on chromosome 3. 1 …

Clinical case A 29-year-old female with bilateral retinal capillary haemangiomas (RCH). A
genetic analysis was carried out due to the suspicion of von Hippel–Lindau (VHL) disease …

Introdução: No presente trabalho iremos discorrer sobre a doença de von Hippel-Lindau
(VHL). A VHL é uma doença hereditária rara, que afeta, aproximadamente, 1 em cada …

Abstract von Hippel Lindau (VHL) disease is caused by inactivation of the VHL tumor
suppressor gene, resulting in formation of multiple systemic tumors. Juxtapapillary retinal …

Introduction Retinal hemangioblastoma is one of the most common tumors in von Hippel-
Lindau disease. In addition to the classical pathological characteristics of von Hippel-Lindau …