alexa von Hippel-Lindau disease: a clinical and scientific review.
Oncology

Oncology

Journal of Brain Tumors & Neurooncology

Author(s): Maher ER, Neumann HP, Richard S

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Abstract The autosomal dominantly inherited disorder von Hippel-Lindau disease (VHL) is caused by germline mutations in the VHL tumour suppressor gene (TSG). VHL mutations predispose to the development of a variety of tumours (most commonly retinal and central nervous system haemangioblastomas, clear cell renal carcinoma and phaeochromocytomas). Here, we review the clinical and genetic features of VHL disease, briefly review the molecular pathogenesis and outline clinical management and tumour surveillance strategies.
This article was published in Eur J Hum Genet and referenced in Journal of Brain Tumors & Neurooncology

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