Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous Malformation

Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous Malformation

Background Familial cerebral cavernous alformation (CCM) is an autosomal dominant disease caused by mutations in KRIT1, CCM2, or PDCD10. Cases typically present with multiple lesions, strong family history, and neurological symptoms, including seizures, headaches, or other deficits. Intracranial hem...

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Bibliographic Details
Main Authors: Shantel Weinsheimer, Jeffrey Nelson, Adib A. Abla, Nerissa U. Ko, Cynthia Tsang, Obiora Okoye, Joseph M. Zabramski, Amy Akers, Atif Zafar, Marc C. Mabray, Blaine L. Hart, Leslie Morrison, Charles E. McCulloch, Helen Kim
Format: Article
Language:English
Published: Wiley 2023-02-01
Series:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Subjects:
cerebral cavernous malformation
familial
hemorrhage
risk factor
Online Access:https://www.ahajournals.org/doi/10.1161/JAHA.122.027572

Internet

https://www.ahajournals.org/doi/10.1161/JAHA.122.027572

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