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 (FBN1). Cardinal clinical phenotypes of MFS are highly variable in terms of severity, and commonly involve cardiovascular, ocular,...

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Detalles Bibliográficos
Autores principales: Marelli, Susan, Micaglio, Emanuele, Taurino, Jacopo, Salvi, Paolo, Rurali, Erica, Perrucci, Gianluca L., Dolci, Claudia, Udugampolage, Nathasha Samali, Caruso, Rosario, Gentilini, Davide, Trifiro’, Giuliana, Callus, Edward, Frigiola, Alessandro, De Vincentiis, Carlo, Pappone, Carlo, Parati, Gianfranco, Pini, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340634/
https://www.ncbi.nlm.nih.gov/pubmed/37443678
http://dx.doi.org/10.3390/diagnostics13132284

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