Intracerebral haemorrhage in CADASIL. A case report.

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.

journal_name

Acta Neurol Belg

journal_title

Acta neurologica Belgica

authors

Werbrouck BF,De Bleecker JL

subject

Has Abstract

pub_date

2006-12-01 00:00:00

pages

219-21

issue

4

eissn

0300-9009

issn

2240-2993

journal_volume

106

pub_type

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