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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|Series:||Journal of Ophthalmic & Vision Research|