Alport Syndrome with Progressive Decrease in Retinal Thickness: A Case Report

Author:

Lee Yu Ri1,Chung Kyu Ho2,Lee Jee Hye1,Choi Jin2

Affiliation:

1. Department of Ophthalmology, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, Korea

2. Republic of Korea Air Force The 8948th Unit, Hwacheon, Korea

Publisher

The Korean Retina Society

Subject

General Medicine

Reference10 articles.

1. HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS

2. Expert Guidelines for the Management of Alport Syndrome and Thin Basement Membrane Nephropathy

3. Ocular Features in Alport Syndrome: Pathogenesis and Clinical Significance

4. Zhou J, Hertz JM, Tryggvason K. Mutation in the alpha 5(IV) collagen chain in juvenile-onset Alport syndrome without hearing loss or ocular lesions: detection by denaturing gradient gel electrophoresis of a PCR product. Am J Hum Genet 1992;50:1291-300.

5. Renal, auricular, and ocular outcomes of Alport syndrome and their current management

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