Acute myeloid leukemia in a 38-year-old hemodialyzed patient with von Hippel-Lindau disease

Von Hippel-Lindau disease (VHL disease) is a hereditary cancer predisposition syndrome caused by mutations of the von Hippel-Lindau tumor suppressor gene. The gene product, pVHL, regulates the level of proteins that play a central role in protecting cells against hypoxia. Clinical hallmarks of von H...

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Detalles Bibliográficos
Autores principales: Labno-Kirszniok, Katarzyna, Nieszporek, Teresa, Wiecek, Andrzej, Helbig, Grzegorz, Lubinski, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846582/
https://www.ncbi.nlm.nih.gov/pubmed/23968328
http://dx.doi.org/10.1186/1897-4287-11-11

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846582/
https://www.ncbi.nlm.nih.gov/pubmed/23968328
http://dx.doi.org/10.1186/1897-4287-11-11

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