Keratoconus in a patient with Alport syndrome: A case report

被引:0
|
作者
Majid Moshirfar [1 ,2 ,3 ]
David F Skanchy [4 ]
Aaron T Gomez [5 ]
Yasmyne C Ronquillo [3 ]
Benjamin Buckner [3 ]
Phillip C Hoopes [3 ]
机构
[1] John A. Moran Eye Center, Department of Ophthalmology and Visual Sciences, University of Utah School of Medicine
[2] Kellogg Eye Center, Department of Ophthalmology, University of Michigan Medical School
[3] The University of Texas Rio Grande Valley School of Medicine
关键词
Alport syndrome; Keratoconus; Type; Ⅳ; collagen; COL4A genes; Corneal ectasia; Case report;
D O I
暂无
中图分类号
R692.3 [肾炎]; R772.2 [角膜疾病];
学科分类号
1002 ; 100210 ; 100212 ;
摘要
BACKGROUND Known ocular manifestations of Alport syndrome include features such as anterior lenticonus and fleck retinopathy. Reports of keratoconus in such patients are limited. We report tomographic findings consistent with keratoconus in a patient with Alport syndrome.CASE SUMMARY A 52-year-old female was referred to our ophthalmology clinic with decreased vision and increased tearing. She was diagnosed with stage Ⅲ Alport syndrome two years prior. Upon examination she was found to have average keratometries of 48D bilaterally with tomographic evidence of keratoconus.CONCLUSION Although a rare presentation, concurrent Alport syndrome and keratoconus should be considered when reviewing the ocular health of Alport syndrome patients and appropriate management steps should be taken upon the diagnosis.
引用
收藏
页码:3012 / 3017
页数:6
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