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From arterial hypertension complications to von Hippel-Lindau syndrome diagnosis
Von Hippel-Lindau syndrome is a rare, genetically based, autosomal dominant disorder. Its course is accompanied by the development of multiple neoplasms with the following tumours diagnosed most commonly in the central nervous system haemangioblastoma, clear cell renal cell carcinoma, phaeochromocyt...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535675/ https://www.ncbi.nlm.nih.gov/pubmed/26268347 http://dx.doi.org/10.1186/s13052-015-0158-y |