Cargando…
Case Report: Morphological Characterization and Long-Term Observation of Bilateral Sequential Internal Mammary Artery Aneurysms in a Patient With Confirmed FBN1 Mutation
Marfan syndrome (MFS) is a genetically determined connective tissue disorder that leads to ocular, skeletal, and severe cardiovascular involvement. High mortality of MFS is associated with aortic dissection and aneurysm characteristic to the syndrome. In MFS, only a few cases of peripheral arterial...
Autores principales: | Stengl, Roland, Ágg, Bence, Szilveszter, Bálint, Benke, Kálmán, Daradics, Noémi, Ruskó, Bernadett, Vattay, Borbála, Merkely, Béla, Pólos, Miklós, Szabolcs, Zoltán |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8242161/ https://www.ncbi.nlm.nih.gov/pubmed/34222386 http://dx.doi.org/10.3389/fcvm.2021.697591 |
Ejemplares similares
-
Increased visceral arterial tortuosity in Marfan syndrome
por: Ágg, Bence, et al.
Publicado: (2020) -
Possible extracardiac predictors of aortic dissection in Marfan syndrome
por: Ágg, Bence, et al.
Publicado: (2014) -
Potential predictors of severe cardiovascular involvement in Marfan syndrome: the emphasized role of genotype–phenotype correlations in improving risk stratification—a literature review
por: Stengl, Roland, et al.
Publicado: (2021) -
Bentall procedure: quarter century of clinical experiences of a single surgeon
por: Benke, Kálmán, et al.
Publicado: (2016) -
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement
por: Stengl, Roland, et al.
Publicado: (2020)