Skip to main content Accessibility help
×
Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-12-01T02:54:30.862Z Has data issue: false hasContentIssue false

Chapter 5.1 - Chapter

from 5 - Hereditary and Genetic Causes of Stroke

Published online by Cambridge University Press:  06 October 2022

Anita Arsovska
Affiliation:
University of Ss Cyril and Methodius
Derya Uluduz
Affiliation:
Istanbul Üniversitesi
Get access

Summary

Marfan syndrome is a genetically inherited systemic disease of connective tissue, usually characterized by skeletal, cardiovascular and ocular involvement. We present a 44 years-old male, with heart valve and lens subluxation surgery, presented to the outpatient clinic with complaint of weakness on the left side. He was receiving anticoagulant treatment. His parents were second-degree relatives, and his 16-years-old son had aortic valve regurgitation and lens subluxation. The patient was extremely tall and thin with typical musculoskeletal features of Marfan syndrome. These included pectus excavatus deformity, ulnar deviation in both hands, as well as swan neck deformity, long fingers, joint hypermobility, and right-sided scoliosis. Neurological examination revealed irregular pupil on the right, left-sided hemiparesis, hyperreflexia, and piramidal signs on the left side. Brain magnetic resonance imaging showed infarction in the temporo-parietal region of the right hemisphere

Type
Chapter
Information
Rare Causes of Stroke
A Handbook
, pp. 206 - 211
Publisher: Cambridge University Press
Print publication year: 2022

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Meester, JAN, Verstraeten, A, Schepers, D, et al. Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome. Ann Cardiothorac Surg. 2017;6(6): 582594.CrossRefGoogle ScholarPubMed
Sakai, LY, Keene, DR, Renard, M, De Backer, J. FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders. Gene. 2016;591(1): 279291.CrossRefGoogle ScholarPubMed
Yuan, S-M, Jing, H. Marfan’s syndrome: an overview. Sao PaoloMed J. 2010;128(6): 360366.CrossRefGoogle ScholarPubMed
Pepe, G, Giusti, B, Sticchi, E, et al. Marfan syndrome: current perspectives. Appl Clin Genet. 2016;9: 5565.CrossRefGoogle ScholarPubMed
Loeys, BL, Dietz, CH, Braverman, AC, et al. The revised Ghent nosology for the Marfan syndrome. J Med Genet. 2010;47(7): 476485.CrossRefGoogle ScholarPubMed
Kumar, A, Agarwal, S. Marfan syndrome: an eyesight of syndrome. Meta Gene. 2014;2: 96105.CrossRefGoogle ScholarPubMed
vonKodolitsch, Y, De Backer, J, Schüler, H, et al. Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome. Appl Clin Genet. 2015;8:137–55.Google Scholar
Tinkle, BT, Saal, HM, and Committee on Genetics. Health supervision for children with Marfan syndrome. Pediatrics. 2013;132(4):e1059–72.CrossRefGoogle ScholarPubMed
Ozyurt, A, Baykan, A, Argun, M, et al. Early onset Marfan syndrome: Atypical clinical presentation of two cases. Balkan J Med Genet. 2015;18(1): 7176.CrossRefGoogle ScholarPubMed
CSANZ Cardiovascular Genetics Working Group, Ades, L. Guidelines for the diagnosis and management of Marfan syndrome. Heart Lung Circ. 2007;16(1): 2830.CrossRefGoogle ScholarPubMed
Pyeritz, R. Evaluation of the adolescent or adult with some features of Marfan syndrome. Genet Med. 2012;14(1): 171177.CrossRefGoogle ScholarPubMed
Ha, HI, Seo, JB, Lee, SH, et al. Imaging of Marfan syndrome: Multisystemic manifestations. Radiographics. 2007;27(4): 9891004.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

  • Chapter
  • Edited by Derya Uluduz, Istanbul Üniversitesi
  • Anita Arsovska
  • Book: Rare Causes of Stroke
  • Online publication: 06 October 2022
  • Chapter DOI: https://doi.org/10.1017/9781108902793.036
Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • Chapter
  • Edited by Derya Uluduz, Istanbul Üniversitesi
  • Anita Arsovska
  • Book: Rare Causes of Stroke
  • Online publication: 06 October 2022
  • Chapter DOI: https://doi.org/10.1017/9781108902793.036
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Chapter
  • Edited by Derya Uluduz, Istanbul Üniversitesi
  • Anita Arsovska
  • Book: Rare Causes of Stroke
  • Online publication: 06 October 2022
  • Chapter DOI: https://doi.org/10.1017/9781108902793.036
Available formats
×