Marfan Syndrome: Enhanced Diagnostic Tools and Follow-up Management Strategies.
Fibrillin-1
Marfan syndrome
connective tissue disease
multidisciplinary approach
personalized medicine
Journal
Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402
Informations de publication
Date de publication:
05 Jul 2023
05 Jul 2023
Historique:
received:
13
06
2023
revised:
01
07
2023
accepted:
03
07
2023
medline:
14
7
2023
pubmed:
14
7
2023
entrez:
14
7
2023
Statut:
epublish
Résumé
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 (
Identifiants
pubmed: 37443678
pii: diagnostics13132284
doi: 10.3390/diagnostics13132284
pmc: PMC10340634
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Subventions
Organisme : Ministero della Salute
ID : Ricerca Corrente
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