OCULAR MANIFESTATIONS OF ALPORT SYNDROME: A CASE STUDY

Kelly Schoorens

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Abstract

Alport syndrome is an inherited basement membrane disorder characterized by nephritis, hearing loss and distinct ocular findings resulting from collagen gene mutations. The following case demonstrates the characteristic ocular and systemic manifestations of Alport syndrome.

Details

Year: 2016

Program Number: R2016169

Author Affiliation: New England College of Optometry

Co-Authors: n/a

Co-Author Affiliation: n/a

Room: Ballroom A-B