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VHLDVon Hippel-Lindau Disease
References in periodicals archive ?
Von Hippel-Lindau disease (VHL), also known as Familial cerebello retinal angiomatosis, is a rare genetic disorder characterised by visceral cysts and benign tumours with potential for subsequent malignant transformation.
Transpupillary Thermotherapy for Retinal Capillary Hemangiomas in Von Hippel-Lindau Disease.
Prevalence, morphology and biology of renal cell carcinoma in von Hippel-Lindau disease compared to sporadic renal cell carcinoma.
The natural history of hemangioblastomas of the central nervous system in patients with von Hippel-Lindau disease.
Identification of the von Hippel-Lindau disease tumor suppressor gene.
Milenka, from Chile, has Von Hippel-Lindau disease which is a rare inherited genetic condition.
Von Hippel-Lindau disease (VHL) is a rare, genetic multi-system disorder characterised by the abnormal growth of tumours (angiomatosis) in certain parts of the body.
Elaine suffers from pre-cancerous cysts and tumours caused by the extremely rare von Hippel-Lindau disease (VHL).
Exactly a year ago, both Elaine's kidneys were removed because of pre- cancerous cysts and tumours caused by the extremely rare von Hippel-Lindau disease (VHL).
Von Hippel-Lindau disease is a hereditary cancer syndrome caused by a germline mutation in or deletion of the VHL gene, and patients are at risk for developing tumors and fluid-filled sacs (cysts) in a number of organs.
Multiple neuroendocrine tumors of the pancreas in von Hippel-Lindau disease patients: histopathological and molecular genetic analysis.