Literature DB >> 17273695

[Posterior amorphous corneal dystrophy: case report].

Lauro Augusto de Oliveira1, Luiz Antônio Vieira, Denise de Freitas, Luciene Barbosa de Sousa.   

Abstract

The purpose of this paper is to warn the ophthalmologist about the possibility of facing rare cases of corneal dystrophies. Clinical findings of a case of posterior amorphous dystrophy were correlated with refraction, topography, and ultrasound biomicroscopy.

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Year:  2006        PMID： 17273695     DOI： 10.1590/s0004-27492006000600029

Source DB:  PubMed          Journal:  Arq Bras Oftalmol        ISSN： 0004-2749            Impact factor:   0.872


  3 in total

1.  Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.

Authors:  Anthony J Aldave; George O D Rosenwasser; Vivek S Yellore; Jeanette C Papp; Eric M Sobel; Michele N Pham; Michael C Chen; Sugandha Dandekar; Ram Sripracha; Sylvia A Rayner; Joseph W Sassani; Michael B Gorin
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-03-31       Impact factor: 4.799

2.  Confirmation and refinement of the heterozygous deletion of the small leucine-rich proteoglycans associated with posterior amorphous corneal dystrophy.

Authors:  Aleck E Cervantes; Katherine M Gee; Martha F Whiting; Ricardo F Frausto; Anthony J Aldave
Journal:  Ophthalmic Genet       Date:  2018-04-19       Impact factor: 1.803

3.  Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12.

Authors:  Michelle J Kim; Ricardo F Frausto; George O D Rosenwasser; Tina Bui; Derek J Le; Edwin M Stone; Anthony J Aldave
Journal:  PLoS One       Date:  2014-04-23       Impact factor: 3.240
  3 in total

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