A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy
Many types of inherited renal diseases have ocular features that occasionally support a diagnosis. The following study describes an unusual example of a 40-year-old woman with granular corneal dystrophy type II complicated by renal involvement. These two conditions may coincidentally coexist; howeve...
Main Authors: | , , , , , |
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Format: | Online |
Language: | English |
Published: |
S. Karger AG
2016
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073658/ |