Von Hippel-lindau | search
Click here to view Von Hippel-lindau news from 60+ newspapers.
Bookmark or Share- Von Hippel–Lindau disease - WikipediaVon Hippel–Lindau disease (VHL), also known as Von Hippel–Lindau syndrome, is a rare genetic disorder with multisystem involvement. [3] It is characterized by visceral cysts and benign tumors with potential for subsequent malignant transformation.
- Von Hippel-Lindau Disease (VHL) | National Institute of Neurological ...What is Von Hippel-Lindau disease (VHL)? Von Hippel-Lindau disease (VHL) is a rare, genetic multi-system disorder in which non-cancerous tumors grow in certain parts of the body. Slow-growing hemgioblastomas—benign tumors with many blood vessels—may develop in the:
- von Hippel-Lindau Disease (VHL) - Cleveland Clinicvon Hippel-Lindau syndrome is an inherited disorder that may happen when one of your biological parents passes on an abnormal version of the VHL gene, a tumor suppressor gene that manages cell growth.
- Von Hippel-Lindau disease | Radiology Reference Article - Radiopaedia.orgVon Hippel-Lindau (vHL) disease is characterized by the development of numerous benign and malignant tumors in different organs (at least 40 types 1) due to mutations in the VHL tumor suppressor gene on chromosome 3.
- Von Hippel-Lindau (VHL) - Johns Hopkins MedicineVon Hippel-Lindau (VHL) syndrome is a rare disorder caused by a mutation in a single gene called the VHL gene. If you have VHL syndrome, you are at greater risk of developing certain tumors. VHL Syndrome: What You Need to Know. VHL syndrome affects one in 36,000 people.
More
