Literature DB >> 301357

Meesmann's epithelial dystrophy of the cornea.

B S Fine, M Yanoff, E Pitts, F D Slaughter.   

Abstract

Two separate pedigrees had typical Meesmann's dystrophy of the corneal epithelium. Histologic examination of one patient from each pedigree showed two characteristic findings in corneal epithelium; the previously designated "peculiar substance" in the cells, and the vacuolated homogeneous substance mostly within the cysts. The primary disturbance probably involves the cytoplasmic ground substance that ultimately may result in complete homogenization of cells and the formation of cysts. Thickening of the epithelial basement membrane is variable and is a nonspecific response by the epithelial basal cells.

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Year:  1977        PMID: 301357     DOI: 10.1016/0002-9394(77)90128-3

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  13 in total

Review 1.  Unilateral Meesmann's dystrophy.

Authors:  A Goldberg; U Schlötzer-Schrehardt; T Seiler
Journal:  Int Ophthalmol       Date:  1997       Impact factor: 2.031

2.  The basement membrane complex of the human corneal epithelium.

Authors:  H Brewitt; E Reale
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1981

3.  A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy.

Authors:  L D Corden; O Swensson; B Swensson; R Rochels; B Wannke; H J Thiel; W H McLean
Journal:  Br J Ophthalmol       Date:  2000-05       Impact factor: 4.638

4.  Cogan's microcystic dystrophy of the cornea: ultrastructure and photomicroscopy.

Authors:  A J Dark
Journal:  Br J Ophthalmol       Date:  1978-12       Impact factor: 4.638

5.  Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.

Authors:  H Hassan; C Thaung; N D Ebenezer; G Larkin; A J Hardcastle; S J Tuft
Journal:  Eye (Lond)       Date:  2012-12-07       Impact factor: 3.775

6.  A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy.

Authors:  Takahiko Seto; Keiko Fujiki; Hitoshi Kishishita; Takuro Fujimaki; Akira Murakami; Atsushi Kanai
Journal:  Jpn J Ophthalmol       Date:  2008-07-27       Impact factor: 2.447

7.  Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann's corneal dystrophy in a German family.

Authors:  Ina Clausen; Gernot I W Duncker; Claudia Grünauer-Kloevekorn
Journal:  Mol Vis       Date:  2010-05-29       Impact factor: 2.367

8.  A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy.

Authors:  M K Yoon; J F Warren; D S Holsclaw; D C Gritz; T P Margolis
Journal:  Br J Ophthalmol       Date:  2004-06       Impact factor: 4.638

Review 9.  Corneal dystrophies.

Authors:  Gordon K Klintworth
Journal:  Orphanet J Rare Dis       Date:  2009-02-23       Impact factor: 4.123

10.  A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.

Authors:  Lori S Sullivan; Eric B Baylin; Ramon Font; Stephen P Daiger; Jay S Pepose; Thomas E Clinch; Hisashi Nakamura; Xinping C Zhao; Richard W Yee
Journal:  Mol Vis       Date:  2007-06-21       Impact factor: 2.367

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