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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Bibliographic Details
Main Authors: Hamed Esfandiari, Shabnam Ansari, Hossein Mohammad-Rabei, Marilyn B Mets
Format: Article
Published: Knowledge E 2019-01-01
Series:Journal of Ophthalmic & Vision Research
Online Access:;year=2019;volume=14;issue=1;spage=71;epage=77;aulast=Esfandiari