Natural history of familial cerebral cavernous malformations: the CCM_Italia cohort study

BackgroundFamilial cerebral cavernous malformations (fCCMs) are a rare genetic autosomal dominant cerebrovascular disease characterized by multiple cerebral and spinal angiomas. The condition is caused by mutations in KRIT1 (CCM1), CCM2 (malcavernin), or PDCD10 (CCM3) and may lead to intracerebral h...

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Principais autores:	Silvia Lanfranconi, Elisa Scola, Deborah Novelli, Anna Poggesi, Francesca Pescini, Marco Pavanello, Ferruccio Romano, Quintino Giorgio D’Alessandris, Walter Marani, Francesco Signorelli, Giorgio Iaconetta, Giovanni Torelli, Enrico Fainardi, Mariasavina Severino, Luigi Gianmaria Remore, Giulio Andrea Bertani, Giorgio Conte, Valeria Capra, Antonella Vasamì, Enrico Nicolis, Giorgia Contino, Dario Ronchi, Maria Chiara Palmieri, Alessandra Previtali, Pier Paolo Mattogno, Carmelo Lucio Sturiale, Maria Elena Solarino, Rita Caliulo, Maria Teresa Bozzi, Filippo Fratini, Elisa R. Zanier, Roberto Latini, Jennifer Marie Theresia Anna Meessen, Marco Locatelli, and the CCM_Italia investigators
格式:	Artigo
语言:	Inglês
出版:	Frontiers Media S.A. 2026-01-01
丛编:	Frontiers in Neurology
主题:	cerebral cavernous malformation familial cerebral cavernous malformation intracerebral heamorrhage focal neurological deficit registry
在线阅读:	https://www.frontiersin.org/articles/10.3389/fneur.2025.1668098/full
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