Von Hippel-Lindau disease
Von Hippel–Lindau disease is a rare, autosomal dominant genetic condition that predisposes individuals to benign and malignant tumours. The most common tumours found in VHL are central nervous system and retinal hemangioblastomas, clear cell renal carcinomas, pheochromocytomas, pancreatic neuroendocrine tumours, pancreatic cysts, endolymphatic sac tumors and epididymal papillary cystadenomas. VHL results from a mutation in the von Hippel–Lindau tumor suppressor gene on chromosome 3p25.3.
U.S. National Library of Medicine
von Hippel-Lindau Disease
An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions.
The numerical value of von hippel-lindau disease in Chaldean Numerology is: 9
The numerical value of von hippel-lindau disease in Pythagorean Numerology is: 6
Images & Illustrations of von hippel-lindau disease
Find a translation for the von hippel-lindau disease definition in other languages:
Select another language:
Discuss these von hippel-lindau disease definitions with the community:
Word of the Day
Would you like us to send you a FREE new word definition delivered to your inbox daily?
Use the citation below to add this definition to your bibliography:
"von hippel-lindau disease." Definitions.net. STANDS4 LLC, 2018. Web. 23 Jan. 2018. <http://www.definitions.net/definition/von hippel-lindau disease>.