Marfan Syndrome beyond Aortic Root—Phenotyping Using Cardiovascular Magnetic Resonance Imaging and Clinical Implications

Marfan Syndrome beyond Aortic Root—Phenotyping Using Cardiovascular Magnetic Resonance Imaging and Clinical Implications

Marfan syndrome (MFS) is an inherited autosomal-dominant connective tissue disorder with multiorgan involvement including musculoskeletal, respiratory, cardiovascular, ocular, and skin manifestations. Life expectancy in patients with MFS is primarily determined by the degree of cardiovascular involv...

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Chi tiết về thư mục
Những tác giả chính: Evangelia Nyktari, Maria Drakopoulou, Panagiotis Rozos, Sofia Loukopoulou, Thomas Vrachliotis, Soultana Kourtidou, Konstantinos Toutouzas
Định dạng: Bài viết
Ngôn ngữ:English
Được phát hành: MDPI AG 2023-05-01
Loạt:Medicina
Những chủ đề:
Marfan syndrome
arrhythmias
heart failure
cardiomyopathy
cardiovascular magnetic resonance imaging
Truy cập trực tuyến:https://www.mdpi.com/1648-9144/59/5/942

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https://www.mdpi.com/1648-9144/59/5/942

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