von Hippel-Lindau Syndrome: Genetic Study of Case With a Rare Pathogenic Variant With Optic Nerve Hemangioblastoma, a Rare Phenotypic Expression

von Hippel-Lindau syndrome (VHLS) is a rare, autosomal dominant genetic disease with high penetrance and variable phenotypic expression caused by variants in the VHL gene. VHLS is associated with the presence of vascular tumors, often hemangioblastoma of the central nervous system, retina, or spinal...

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Bibliographic Details
Main Authors: Sandra Di Felice Boratto, Pedro Augusto Soffner Cardoso, Denise Gonçalves Priolli, Ricardo Vieira Botelho, Alberto Goldenberg, Bianca Bianco, Jaques Waisberg
Format: Artigo
Language:Inglês
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Oncology
Subjects:
von Hippel-Lindau syndrome
hemangioblastoma
optic nerve neoplasms
brain neoplasms
renal carcinoma
VHL gene
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2020.00139/full
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