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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Bibliografiska uppgifter
Huvudupphovsmän: Sandra Di Felice Boratto, Pedro Augusto Soffner Cardoso, Denise Gonçalves Priolli, Ricardo Vieira Botelho, Alberto Goldenberg, Bianca Bianco, Jaques Waisberg
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2020-02-01
Serie:Frontiers in Oncology
Ämnen:
von Hippel-Lindau syndrome
hemangioblastoma
optic nerve neoplasms
brain neoplasms
renal carcinoma
VHL gene
Länkar:https://www.frontiersin.org/article/10.3389/fonc.2020.00139/full
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