Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhage
Journal
European Journal of Neurology
Journal Volume
29
Journal Issue
11
Pages
3243
End Page
3254
ISSN
1351-5101
Date Issued
2022-11
Author(s)
Chu, Yung-Tsai
Ko, Tzu-Yu
Abstract
The NOTCH3 mutation is a common cause of hereditary cerebral small vessel disease (CSVD) and may be a cause of spontaneous intracerebral haemorrhage (ICH). The aim was to investigate the clinical/imaging features for identifying the NOTCH3-mutation-related ICH.
Subjects
NOTCH3; CADASIL; MRI; cerebral microbleed; intracerebral haemorrhage
SDGs
Publisher
WILEY
Type
journal article