Article

Acute ischemic stroke leading to a diagnosis of Marfan syndrome: Case report and systematic review

2023-03-30

Abstract excerpt

Neurologic deficiency is a rare manifestation of dominantly inherited Marfan syndrome (MFS), which is caused by mutation of the gene encoding fibrillin 1 (FBN1) and characterized by cardiovascular and musculoskeletal abnormalities. Intravenous thrombolysis is the standard of care for acute ischemic stroke (AIS) but its safety in individuals with MFS is unknown. Here we report 3 cases of MFS presenting with AIS. Tw...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: ae9f7f63-acd6-5b21-bd85-0497e2f76177
DOI: 10.21203/rs.3.rs-2707677/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Acute ischemic stroke leading to a diagnosis of Marfan syndrome: Case report and systematic reviewDOI 10.21203/rs.3.rs-2707677/v1Read

Focal cerebral arteriopathy in adults: A single centre experienceSemantic proximity Read

[Latest advances in the diagnosis and treatment of Marfan syndrome].Semantic proximity Read

Ischemic Stroke in a COVID-19-Infected Patient: A Case Report and Literature ReviewSemantic proximity Read

[Clinical aspects of Marfan syndrome].Semantic proximity Read

[Marfan syndrome: strategies of interdisciplinary care].Semantic proximity Read

[Multidisciplinary practice guideline 'Marfan syndrome'].Semantic proximity Read

Diagnosis and treatment of Marfan syndrome: an update.Semantic proximity Read

Marfan Syndrome: A Clinical Update.Semantic proximity Read

[Marfan syndrome].Semantic proximity Read

[Marfan's syndrome. Clinical and molecular characterization of 51 Italian patients].Semantic proximity Read

Update on stroke.Semantic proximity Read

Cerebral venous sinus thrombosis associated with JAK2 V617F mutation-related pre-primary myelofibrosis: a case report and literature review.Semantic proximity Read