Temporal lobe pleomorphic xanthoastrocytoma and acquired BRAF mutation in an adolescent with the constitutional 22q11.2 deletion syndrome

DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional microdeletion at chromosome 22q11.2. While rare cases of malignancy have been described, likely due to underlying immunodeficiency, central nervous s...

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Bibliografiska uppgifter
Huvudupphovsmän: Murray, Jeffrey C., Donahue, David J., Malik, Saleem I., Dzurik, Yvette B., Braly, Emily Z., Dougherty, Margaret J., Eaton, Katherine W., Biegel, Jaclyn A.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2010
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2998545/
https://ncbi.nlm.nih.gov/pubmed/20730472
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11060-010-0350-2
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