Literature DB >> 300621

Lattice corneal dystrophy. Report of an unusual case.

M Yanoff, B S Fine, N J Colosi, J A Katowitz.   

Abstract

The clinical, histochemical, light and electron microscopic evaluation of a case of lattice corneal dystrophy, appears clinically as an atypical granular dystrophy. There is structural and histochemical differentiation of the two dystrophies. Electron microscopy is often an invaluable aid in establishing a definitive diagnosis. The possible sources of the filamentous material found in lattice corneal dystrophy are discussed. It seems that not only keratocytes, but also corneal epithelial cells, occasionally may have the ability to elaborate the abnormal material that is considered to be amyloid in nature.

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Year:  1977        PMID: 300621     DOI: 10.1001/archopht.1977.04450040117018

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


  4 in total

1.  Granular and lattice deposits in corneal dystrophy caused by R124C mutation of TGFBIp.

Authors:  Dhara A Patel; Shu-Hong Chang; George J Harocopos; Smita C Vora; Diep Huu Thang; Andrew J W Huang
Journal:  Cornea       Date:  2010-11       Impact factor: 2.651

2.  Bilateral recurrence of granular corneal dystrophy in the grafts. A clinico-pathologic study.

Authors:  H Witschel; R Sundmacher
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1979-01-15

3.  Superficial reticular degeneration of Koby.

Authors:  H D Perry; H G Scheie
Journal:  Br J Ophthalmol       Date:  1980-11       Impact factor: 4.638

4.  Corneal elastosis within lattice dystrophy lesions.

Authors:  J Pe'er; B S Fine; A Dixon; D S Rothberg
Journal:  Br J Ophthalmol       Date:  1988-03       Impact factor: 4.638

  4 in total

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