Literature DB >> 6983339

The ultrastructure of Descemet's membrane. III. Fuchs' dystrophy.

W M Bourne, D H Johnson, R J Campbell.   

Abstract

The ultrastructure of Descemet's membrane was studied by transmission electron microscopy in corneal buttons removed from 11 phakic eyes with Fuchs' dystrophy. Abnormalities in Descemet's membrane consistent with abnormal endothelial function early in life (prior to age 20 years) were present in all corneas. Thus, despite the relatively late clinical onset of Fuch's dystrophy, endothelial abnormalities are present quite early in life in this disease. An abnormal fibrillar layer was thicker in those corneas with greater stromal and epithelial edema, possibly indicating that this layer is formed mainly during periods of endothelial decompensation.

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Year:  1982        PMID： 6983339     DOI： 10.1001/archopht.1982.01030040932013

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


  21 in total

Review 1.  Biomechanical relationships between the corneal endothelium and Descemet's membrane.

Authors:  Maryam Ali; VijayKrishna Raghunathan; Jennifer Y Li; Christopher J Murphy; Sara M Thomasy
Journal:  Exp Eye Res       Date:  2016-09-14       Impact factor: 3.467

Review 2.  Graft survival and endothelial outcomes in the new era of endothelial keratoplasty.

Authors:  Sanjay V Patel
Journal:  Exp Eye Res       Date:  2011-06-15       Impact factor: 3.467

3.  Fuchs' corneal dystrophy.

Authors:  Allen O Eghrari; John D Gottsch
Journal:  Expert Rev Ophthalmol       Date:  2010-04

4.  NQO1 downregulation potentiates menadione-induced endothelial-mesenchymal transition during rosette formation in Fuchs endothelial corneal dystrophy.

Authors:  Kishore Reddy Katikireddy; Tomas L White; Taiga Miyajima; Shivakumar Vasanth; Duna Raoof; Yuming Chen; Marianne O Price; Francis W Price; Ula V Jurkunas
Journal:  Free Radic Biol Med       Date:  2017-12-30       Impact factor: 7.376

Review 5.  Fuchs endothelial corneal dystrophy.

Authors:  Hussain Elhalis; Behrooz Azizi; Ula V Jurkunas
Journal:  Ocul Surf       Date:  2010-10       Impact factor: 5.033

6.  Immunohistochemistry and electron microscopy of early-onset fuchs corneal dystrophy in three cases with the same L450W COL8A2 mutation.

Authors:  Cheng Zhang; W Robert Bell; Olof H Sundin; Zenaida De La Cruz; Walter J Stark; W Richard Green; John D Gottsch
Journal:  Trans Am Ophthalmol Soc       Date:  2006

7.  Compositional differences between infant and adult human corneal basement membranes.

Authors:  Andrea Kabosova; Dimitri T Azar; Gregory A Bannikov; Kevin P Campbell; Madeleine Durbeej; Reza F Ghohestani; Jonathan C R Jones; M Cristina Kenney; Manuel Koch; Yoshifumi Ninomiya; Bruce L Patton; Mats Paulsson; Yoshikazu Sado; E Helene Sage; Takako Sasaki; Lydia M Sorokin; Marie-France Steiner-Champliaud; Tung-Tien Sun; Nirmala Sundarraj; Rupert Timpl; Ismo Virtanen; Alexander V Ljubimov
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-11       Impact factor: 4.799

8.  Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.

Authors:  Yi-Ju Li; Mollie A Minear; Xuejun Qin; Jacqueline Rimmler; Michael A Hauser; R Rand Allingham; Robert P Igo; Jonathan H Lass; Sudha K Iyengar; Gordon K Klintworth; Natalie A Afshari; Simon G Gregory
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-06-10       Impact factor: 4.799

9.  Progression and regression of partial corneal involvement in the iridocorneal endothelial syndrome.

Authors:  W M Bourne; R F Brubaker
Journal:  Trans Am Ophthalmol Soc       Date:  1992

Review 10.  Fuchs endothelial corneal dystrophy: The vicious cycle of Fuchs pathogenesis.

Authors:  Stephan Ong Tone; Viridiana Kocaba; Myriam Böhm; Adam Wylegala; Tomas L White; Ula V Jurkunas
Journal:  Prog Retin Eye Res       Date:  2020-05-08       Impact factor: 21.198
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