Literature DB >> 20220350

Diagnosis and management of Marfan syndrome.

Helen D Iams1.   

Abstract

Marfan syndrome (MFS) is a relatively common inherited connective tissue disorder with significant morbidity and mortality. Diagnosis of this syndrome can be difficult, as many of the findings of MFS are present in other syndromes, as well as in the general population. MFS is diagnosed using the Ghent criteria, a group of clinical findings that are specific for MFS. Children and adolescents can pose diagnostic dilemmas as the stigmata of MFS are not present at birth but can evolve through adulthood. Current treatment for MFS is limited to strict blood pressure control and careful selection of physical activity. Aggressive screening and early management could significantly improve the quality of life for these patients.

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Year:  2010        PMID: 20220350     DOI: 10.1249/JSR.0b013e3181d4066c

Source DB:  PubMed          Journal:  Curr Sports Med Rep        ISSN: 1537-890X            Impact factor:   1.733


  3 in total

1.  Characterization of pain, disability, and psychological burden in Marfan syndrome.

Authors:  Traci J Speed; Vani A Mathur; Matthew Hand; Bryt Christensen; Paul D Sponseller; Kayode A Williams; Claudia M Campbell
Journal:  Am J Med Genet A       Date:  2016-11-14       Impact factor: 2.802

2.  Sub-classification of non-inflammatory and inflammatory surgical aortic aneurysms and the association of histological characteristics with potential risk factors.

Authors:  Doina Butcovan; Veronica Mocanu; Raluca Ecaterina Haliga; Beatrice Gabriela Ioan; Mihai Danciu; Grigore Tinica
Journal:  Exp Ther Med       Date:  2019-08-16       Impact factor: 2.447

Review 3.  The Genetics of Thoracic Aortic Aneurysms and Dissection: A Clinical Perspective.

Authors:  Nicolai P Ostberg; Mohammad A Zafar; Bulat A Ziganshin; John A Elefteriades
Journal:  Biomolecules       Date:  2020-01-24
  3 in total

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