We describe a case of von Hippel-Lindau disease (VHL) through three generations of the
same family. First presentation was a young female with a 6-week history of headaches …

INTRODUCTION von Hippel-Lindau (VHL) disease is a rare, multisystem familial neoplasia
syndrome that genetically predisposes affected individuals to tumor formation in multiple …

Abstract Introduction: Von Hippel-Lindau (VHL) syndrome is a disease characterized by the
formation of tumors or cysts in many different parts of the body caused by germline. The …

Von Hippel Lindau (VHL) disease is a rare autosomal dominant condition manifested by
central nervous system hemangioblastoma, retinal angiomas, cysts of pancreas, kidney and …

In recent years advances have been made in the clinical and genetic aspects of von Hippel–
Lindau disease (VHL). Retinal capillary hemangioma is the most common manifestation of …

Von Hippel-Lindau (VHL) disease is an autosomal dominant disorder with high penetrance
characterized by various benign and malignant tumors in multiple organ systems. The …

Abstract Introduction and importance Von Hippel-Lindau (VHL) disease is a rare autosomal
dominantly inherited genetic condition. Von Hippel characterized the illness independently …

A 10-year-old girl was evaluated in the ophthalmologic department for funduscopic
examination because of sustained hypertension, headaches, and vomiting for several …

Von Hippel–Lindau disease (VHL) is an autosomal dominant disorder, caused by mutations
of the VHL gene showing a strong genotype–phenotype correlation. The present report …

A 21-year-old woman presented with a two year history of progressive loss of vision in the
left eye. Brain MRI revealed a supresellar mass felt to be most consistent with a …