Management Strategies of Ocular Abnormalities in Patients with Marfan Syndrome: Current Perspective

Marfan syndrome is an autosomal dominant genetic connective tissue disorder that results from mutations in the fibrillin-1 gene located on chromosome band 15q15–21. Fibrillin, a glycoprotein, is widely expressed throughout the body and contributes to the elasticity and force-bearing capacity of conn...

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Detalles Bibliográficos
Autores principales: Esfandiari, Hamed, Ansari, Shabnam, Mohammad-Rabei, Hossein, Mets, Marilyn B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388525/
https://www.ncbi.nlm.nih.gov/pubmed/30820290
http://dx.doi.org/10.4103/jovr.jovr_29_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388525/
https://www.ncbi.nlm.nih.gov/pubmed/30820290
http://dx.doi.org/10.4103/jovr.jovr_29_18

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