Research Article

Increased Subfoveal Choroidal Thickness and Retinal Structure Changes on Optical Coherence Tomography in Pediatric Alport Syndrome Patients

Table 2

Demographic and clinical findings in patients with Alport syndrome.

NoAgeSexGenetic mutationClinical and OCT findingsSph equ RESph equ LE

117MCOL4A4Unilateral vitelliform lesion+0.75−0.50
218FCOL4A4None−0.250.00
314FCOL4A4None+0.25+0.25
411MCOL4A3None+0.50+0.375
518MCOL4A5Temporal macula thinning−0.75−1.00
616MCOL4A5Temporal macula thinning+0.25−0.75
715FCOL4A4None+0.50+1.00
818MCOL4A5None−0.250.00
99MCOL4A5None−0.375−0.50
1012FCOL4A4None+0.25+0.125
1115MCOL4A4None−0.50−0.25
1212FCOL4A4None+0.75+0.75
1317FCOL4A3None0−0.375
1413MCOL4A4None+0.875+0.625
1513FCOL4A4None+0.25+0.25
1612FCOL4A4None+0.250
1715FCOL4A4None+1.25+1.00
1814FCOL4A3None+0.50+0.25
1916FCOL4A4None+0.125+0.375
2015FCOL4A4None+0.75+0.50
2117MCOL4A3None−0.375−0.875

M: male, F: female, Sph equ: spherical equivalent (diopter), RE: right eye, LE: left eye.