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Intracerebral haemorrhage in CADASIL. A case report
Bart F Werbrouck1, Jan L De Bleecker
1Department of Neurology, Ghent University Hospital, Ghent, Belgium.
Abstract:
CADASIL is an autosomal dominant inherited arteriopathy caused by a point mutation in the Notch3 gene. Classically, it is characterised by recurrent ischemic strokes, often resulting in mental decline. Intracerebral haemorrhages in CADASIL have rarely been reported. We describe a young male with a genetically proven CADASIL who developed an intracerebral haemorrhage while on anticoagulant therapy.
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