Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene

Multiple familial meningiomas occur in rare genetic syndromes, particularly neurofibromatosis type 2. The association of meningiomas and cerebral cavernous malformations (CCMs) has been reported in few patients in the medical literature. The purpose of our study is to corroborate a preferential asso...

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Bibliografiske detaljer
Udgivet i:Neuroradiol J
Main Authors: Garaci, Francesco, Marsili, Luisa, Riant, Florence, Marziali, Simone, Cécillon, Michaelle, Pasquarelli, Roberto, Sangiuolo, Federica, Floris, Roberto, Novelli, Giuseppe, Tournier-Lasserve, Elisabeth, Brancati, Francesco
Format: Artigo
Sprog:Inglês
Udgivet: SAGE Publications 2015
Fag:
Neoplastic Disease
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4757286/
https://ncbi.nlm.nih.gov/pubmed/26246098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1971400915591688
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