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Sunday, June 22, 2008
Abnormal Retinal Blood Vessels in Ehlers-Danlos Syndrome Type VI
Abstract Background Ehlers-Danlos syndrome (EDS) is a hereditary connective tissue disorder caused by defective collagen synthesis and categorized into 11 types based on genetic mutations and clinical features.1 Its principal clinical characteristics include hyperelasticity and vulnerability of the skin and joints to laxity, and fragility of blood vessels.
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