Literature DB >> 21711999

Bilateral iridocorneal endothelial (ICE) syndrome with microspherophakia.

Farrah Islam1, Nadia Azad, Ayesha Khan.   

Abstract

Iridocorneal endothelial syndrome is described to be a rare, usually unilateral ocular condition in young females. There are three known overlapping clinical variants of this condition namely, essential iris atrophy, Cogan-Reese and Chandler syndrome. We report a case of bilateral iridocorneal endothelial (ICE) syndrome with microspherophakia. A 25 years old female presented with microspherophakic lens dislocated into anterior chamber in right eye, and displaced inferiorly in left eye. She was also diagnosed with ICE syndrome and underwent lensectomies in both eyes. This unique combination has never been reported before.

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Year:  2011        PMID: 21711999     DOI: 07.2011/JCPSP.374375

Source DB:  PubMed          Journal:  J Coll Physicians Surg Pak        ISSN: 1022-386X            Impact factor:   0.711


  2 in total

Review 1.  Fuchs endothelial corneal dystrophy and corneal endothelial diseases: East meets West.

Authors:  Y Q Soh; Viridiana Kocaba; Mauricio Pinto; Jodhbir S Mehta
Journal:  Eye (Lond)       Date:  2019-07-02       Impact factor: 3.775

2.  Bilateral Chandler's syndrome: Uncommon entity diagnosed by ultrasound biomicroscopy and confocal microscopy.

Authors:  Parul Ichhpujani; Sushmita Kaushik; Amit Gupta; Surinder S Pandav
Journal:  Indian J Ophthalmol       Date:  2020-03       Impact factor: 1.848

  2 in total

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