First intravenous thrombolysis for pCys194Arg Notch 3 mutation in a Moroccan CADASIL patient with stroke

© 2024 The Authors. Published by Elsevier Inc. on behalf of University of Washington..

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene. Clinical manifestations of CADASIL include lacunar infarcts, transient ischemic attacks, dementia, migraine, and psychiatric disorders. Cerebral MRI can show signal abnormalities in the basal ganglia and white matter, especially characteristic when located in the anterior part of the temporal lobe and external capsules. We report CADASIL patient treated with intravenous tenectelase for acute ischemic stroke, and we present a review of literature aimed to report effectiveness and safety of intravenous thrombolysis in CADASIL patients.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:19

Enthalten in:

Radiology case reports - 19(2024), 6 vom: 28. Apr., Seite 2549-2551

Sprache:

Englisch

Beteiligte Personen:

Mnaili, Mohamed Amine [VerfasserIn]

Links:

Volltext

Themen:

Acute stroke
CADASIL
Case Reports
Thrombolysis intravenous tenecteplase

Anmerkungen:

Date Revised 11.04.2024

published: Electronic-eCollection

Citation Status PubMed-not-MEDLINE

doi:

10.1016/j.radcr.2024.03.006

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM370855124