Abstract
von Hippel Lindau disease (VHL) is an autosomal dominant hereditary disease in which the CNS and retinal hemangioblastomas, renal cell carcinoma, pheocromocytoma, abdominal cystic masses e.g. in the kidney, liver, pancreas, and epididymal cysts may develop. VHL disease manifests itself by 65 years of age. The annual incidence is 1/36,000 live births. In the brain its manifestations are in the cerebellum, brain stem, spinal cord and suprasellar hemangioblastomas and endolymphatic sac tumors.
Keywords
- Renal Cell Carcinoma
- Limb Impairment
- Autosomal Dominant Hereditary Disease
- Epididymal Cyst
- Cerebellar Hemangioblastoma
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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© 2016 Springer International Publishing Switzerland
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Eltorai, I.M. (2016). Spinal Hemangioblastomas in Von Hippel Lindau Disease. In: Rare Diseases and Syndromes of the Spinal Cord. Springer, Cham. https://doi.org/10.1007/978-3-319-45147-3_121
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DOI: https://doi.org/10.1007/978-3-319-45147-3_121
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Online ISBN: 978-3-319-45147-3
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