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December 2021; 7 (6) Clinical/Scientific NotesOpen Access

Novel Mutation of the TGF-β 3 Protein (Loeys-Dietz Type 5) Associated With Aortic and Carotid Dissections

Case Report

Dargham Hussein, Christian Olsson, Kristina Lagerstedt-Robinson, View ORCID ProfileTiago Moreira
First published September 15, 2021, DOI: https://doi.org/10.1212/NXG.0000000000000625
Dargham Hussein
From the Department of Neurology (D.H.), Sankt Goran Hospital; Department of Molecular Medicine and Surgery (C.O., K.L.-R.), Karolinska Institutet; Department of Clinical Genetics (K.L.-R.), Department of Cardiovascular Medicine (C.O.), and Department of Neurology (T.M.), Karolinska University Hospital; and Department of Clinical Neuroscience (T.M.), Karolinska Institutet, Stockholm, Sweden.
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  • For correspondence: dargham.hussein@capiostgoran.se
Christian Olsson
From the Department of Neurology (D.H.), Sankt Goran Hospital; Department of Molecular Medicine and Surgery (C.O., K.L.-R.), Karolinska Institutet; Department of Clinical Genetics (K.L.-R.), Department of Cardiovascular Medicine (C.O.), and Department of Neurology (T.M.), Karolinska University Hospital; and Department of Clinical Neuroscience (T.M.), Karolinska Institutet, Stockholm, Sweden.
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  • For correspondence: christian.olsson@ki.se
Kristina Lagerstedt-Robinson
From the Department of Neurology (D.H.), Sankt Goran Hospital; Department of Molecular Medicine and Surgery (C.O., K.L.-R.), Karolinska Institutet; Department of Clinical Genetics (K.L.-R.), Department of Cardiovascular Medicine (C.O.), and Department of Neurology (T.M.), Karolinska University Hospital; and Department of Clinical Neuroscience (T.M.), Karolinska Institutet, Stockholm, Sweden.
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  • For correspondence: kristina.lagerstedt-robinson@sll.se
Tiago Moreira
From the Department of Neurology (D.H.), Sankt Goran Hospital; Department of Molecular Medicine and Surgery (C.O., K.L.-R.), Karolinska Institutet; Department of Clinical Genetics (K.L.-R.), Department of Cardiovascular Medicine (C.O.), and Department of Neurology (T.M.), Karolinska University Hospital; and Department of Clinical Neuroscience (T.M.), Karolinska Institutet, Stockholm, Sweden.
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Citation
Novel Mutation of the TGF-β 3 Protein (Loeys-Dietz Type 5) Associated With Aortic and Carotid Dissections
Case Report
Dargham Hussein, Christian Olsson, Kristina Lagerstedt-Robinson, Tiago Moreira
Neurol Genet Dec 2021, 7 (6) e625; DOI: 10.1212/NXG.0000000000000625

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Abstract

Objectives Loeys-Dietz syndrome (LDS) is a rare genetic cause of stroke associated with connective tissue disorders but is not well known among stroke physicians.1 The main objectives of this case report are to increase awareness of this condition and to improve stroke prevention at follow-up visits.

Methods A patient with aortic and carotid artery dissection who had undergone 2 major aortic surgeries with mechanical composite graft and treated with full-dose anticoagulation was reevaluated by neurologists due to retinal hypoperfusion symptoms. After musculoskeletal examination, cervical ultrasonography, and computerized tomography angiography, he was referred for whole-genome sequencing.

Results We found joint hypermobility, skin hyperelasticity, bifid uvula, and combined cervical artery dissections that caused intermittently decreased blood flow in the left ophthalmic artery and an acute asymptomatic embolic stroke. A novel pathogenic variant of LDS type 5 consisting of a heterogeneous nonsense variant c.1044C>A, p.(Cys384*) was found in the TGF-β 3 (TGFB3) gene. Consequently, anticoagulation was intensified, and at 1-year follow-up, the patient's symptoms improved.

Discussion This novel genetic variant coupled to the patient's phenotype contributes to the knowledge of genetic causes of stroke. Patients with multiple arterial dissections and musculoskeletal features should be offered genetic testing and be carefully evaluated to avoid further cerebrovascular ischemic lesions.

Footnotes

  • Go to Neurology.org/NG for full disclosures. Funding information is provided at the end of the article.

  • The Article Processing Charge was funded by the authors.

  • Received April 15, 2021.
  • Accepted in final form August 19, 2021.
  • Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND), which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

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