Marfan Syndrome: Enhanced Diagnostic Tools and Follow-up Management Strategies

Marfan syndrome (MFS) is a rare inherited autosomic disorder, which encompasses a variety of systemic manifestations caused by mutations in the Fibrillin-1 encoding gene (<i>FBN1</i>). Cardinal clinical phenotypes of MFS are highly variable in terms of severity, and commonly involve card...

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出版年:	Diagnostics
主要な著者:	Susan Marelli, Emanuele Micaglio, Jacopo Taurino, Paolo Salvi, Erica Rurali, Gianluca L. Perrucci, Claudia Dolci, Nathasha Samali Udugampolage, Rosario Caruso, Davide Gentilini, Giuliana Trifiro’, Edward Callus, Alessandro Frigiola, Carlo De Vincentiis, Carlo Pappone, Gianfranco Parati, Alessandro Pini
フォーマット:	論文
言語:	英語
出版事項:	MDPI AG 2023-07-01
主題:	Marfan syndrome connective tissue disease multidisciplinary approach personalized medicine Fibrillin-1
オンライン･アクセス:	https://www.mdpi.com/2075-4418/13/13/2284