Literature DB >> 11685064

Unilateral corneal lattice dystrophy.

M S Sridhar1, P R Laibson, R C Eagle, C J Rapuano, E J Cohen.   

Abstract

PURPOSE: To report three cases of seemingly unilateral dystrophy indistinguishable from type I classic lattice corneal dystrophy.
METHODS: Case study of three patients. Three patients, a 31-year-old man, a 44-year-old woman, and a 41-year-old man had multiple lattice lesions in one eye and an apparently healthy fellow eye. Two of these patients underwent penetrating keratoplasty because of poor vision.
RESULTS: Histopathologic examination of the excised corneal button of patient 2 showed amyloid deposits consistent with lattice. In the third patient, lattice lesions were noted in the other eye nearly 13 years after he was first examined.
CONCLUSIONS: Lattice corneal dystrophy is rarely unilateral. Lattice, even in unilateral cases, may cause significant vision loss to warrant penetrating keratoplasty. Lattice lesions may develop in the fellow eye many years later. This possibility should be explained to all patients with apparently unilateral lattice corneal dystrophy.

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Year:  2001        PMID: 11685064     DOI: 10.1097/00003226-200111000-00014

Source DB:  PubMed          Journal:  Cornea        ISSN: 0277-3740            Impact factor:   2.651


  3 in total

1.  Outcomes of keratoplasty in lattice corneal dystrophy in a large cohort of Indian eyes.

Authors:  Ashik Mohamed; Sunita Chaurasia; Muralidhar Ramappa; Somasheila I Murthy; Prashant Garg
Journal:  Indian J Ophthalmol       Date:  2018-05       Impact factor: 1.848

2.  Generation of mouse model of TGFBI-R124C corneal dystrophy using CRISPR/Cas9-mediated homology-directed repair.

Authors:  Kohdai Kitamoto; Yukako Taketani; Wataru Fujii; Aya Inamochi; Tetsuya Toyono; Takashi Miyai; Satoru Yamagami; Masahiko Kuroda; Tomohiko Usui; Yasuo Ouchi
Journal:  Sci Rep       Date:  2020-02-06       Impact factor: 4.379

3.  Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene.

Authors:  Natalie A Afshari; Rosanna P Bahadur; David E Eifrig; Ida B Thogersen; Jan J Enghild; Gordon K Klintworth
Journal:  Mol Vis       Date:  2008-03-12       Impact factor: 2.367

  3 in total

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