Literature DB >> 1078774

Superficial microcystic corneal dystrophy.

M N Luxenberg, B R Friedland, J M Holder.   

Abstract

Microcystic corneal dystrophy was first described in 1964. Since then, several reports have elaborated on the original findings plus other associated corneal changes. The cause is unknown, but pathological studies have been done in several cases. The corneal changes are subtle and easy to miss on routine examination. This study of 17 patients was undertaken to further evaluate the signs and symptoms of this abnormality and to emphasize techniques of examination. Detailed clinical and laboratory evaluations of tear function were performed. No definite association between tear function and the corneal changes could be determined. In this group of patients, the process seemed benign with minimal symptoms.

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Year:  1975        PMID: 1078774     DOI: 10.1001/archopht.1975.01010020113002

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


  4 in total

1.  Recurrent erosion of the cornea.

Authors:  N Brown; A Bron
Journal:  Br J Ophthalmol       Date:  1976-02       Impact factor: 4.638

2.  Microcystic corneal dystrophy.

Authors:  P R Laibson
Journal:  Trans Am Ophthalmol Soc       Date:  1976

3.  Anterior membrane dystrophy following cataract extraction.

Authors:  J D Brodrick
Journal:  Br J Ophthalmol       Date:  1979-05       Impact factor: 4.638

4.  Prevalence of map-dot-fingerprint changes in the cornea.

Authors:  T P Werblin; L W Hirst; W J Stark; I H Maumenee
Journal:  Br J Ophthalmol       Date:  1981-06       Impact factor: 4.638

  4 in total

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