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...
Main Authors: | , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-07-01
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Series: | Diagnostics |
Subjects: | |
Online Access: | https://www.mdpi.com/2075-4418/13/13/2284 |