Keratoconus in a patient with Alport syndrome: A case report

查看全文 作　　者：Majid [1,2,3]Moshirfar;David F [4]Skanchy;Aaron T [5]Gomez;Yasmyne C [3]Ronquillo;Benjamin [3]Buckner;Phillip C [3]Hoopes

机构地区：[1]John A.Moran Eye Center,Department of Ophthalmology and Visual Sciences,University of Utah School of Medicine,Salt Lake City,UT 84101,United States;[2]Utah Lions Eye Bank,Salt Lake City,UT 84101,United States;[3]Hoopes Durrie Rivera Research Center,Hoopes Vision,Draper,UT 84020,United States;[4]Kellogg Eye Center,Department of Ophthalmology,University of Michigan Medical School,Ann Arbor,MI 48103,United States;[5]The University of Texas Rio Grande Valley School of Medicine,Edinburg,TX 78542,United States

出　　处：《World Journal of Clinical Cases》索引2019年第7卷第19期,共6页

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. 关键词：Alport syndrome,Keratoconus Type Ⅳ COLLAGEN COL4A GENES CORNEAL ECTASIA Case report

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Keratoconus in a patient with Alport syndrome: A case report

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