OCULAR MANIFESTATIONS OF ALPORT SYNDROME: A CASE STUDY

Title OCULAR MANIFESTATIONS OF ALPORT SYNDROME: A CASE STUDY
Author, Co-Author Kelly Schoorens
Topic Residents Day
Year
2016
Day
Saturday
Program Number
R2016169
Room
Ballroom A-B
Affiliation
New England College of Optometry
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.

Affiliation of Co-Authors
Outline Kelly_Schoorens.pdf