Literature DB >> 6979375

Meesmann's corneal dystrophy: ultrastructural features.

M Tremblay, I Dubé.   

Abstract

Ultrastructural studies were done on a cornea obtained at the time of lamellar keratoplasty from a patient with the clinical diagnosis of Meesmann's corneal dystrophy. Light microscopy showed in the corneal epithelium the typical tiny cysts containing cellular debris and a homogeneous substance that reacted with periodic acid and Schiff's reagent and stained with Hale's colloidal iron; as well, the basement membrane was markedly thickened. Electron microscopy revealed that the cysts had a corrugated or microvillous wall, consistent with acantholysis. The epithelial cells were rich in glycogen, and many contained the peculiar substance described by others in Meesmann's corneal dystrophy. This substance appeared to be derived from the tonofilaments and was in close relation to the desmosomes. The thick basement membrane showed secondary changes, with one thick zone that was rich in collagen fibrils mimicking abnormal anchoring fibrils and one thin zone that was poor in fibrils but had frequent intercalated fibroblasts and probably represented a repair phenomenon. There was no apparent modification of Bowman's layer or the superficial stroma.

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Year:  1982        PMID: 6979375

Source DB:  PubMed          Journal:  Can J Ophthalmol        ISSN: 0008-4182            Impact factor:   1.882


  6 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.  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

3.  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

4.  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

5.  A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy.

Authors:  A D Irvine; C M Coleman; J E Moore; O Swensson; S J Morgan; J H McCarthy; F J D Smith; G C M Black; W H I McLean
Journal:  Br J Ophthalmol       Date:  2002-07       Impact factor: 4.638

6.  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

  6 in total

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