Literature DB >> 6838805

Bilateral and unilateral mesodermal corneal metaplasia.

V Klauss, K Riedel.   

Abstract

We report on 2 infants, one with a bilateral and the other with a unilateral corneal metaplasia. The first case with bilateral corneal metaplasia showed shortening of both upper and lower lids with formation of symblephara. By ultrasonography the right eye presented with microphthalmos, aphakia, and persistent hyaloid, whereas the inner parts of the left eye appeared to be normal. The question remains to be answered whether this is an abortive cryptophthalmos leading to bilateral corneal metaplasia or a primary corneal metaplasia inhibiting the lid growth. No suggestions concerning the aetiology are made. The second case presented with a unilateral corneal metaplasia, normal eye lids, aphakia, and microphthalmos. This aberration was probably caused by an amniotic band, as it is associated with malformation of the nose on the same side. In case 2 the dermoid was excised and a lamellar corneal graft performed. The histology is reported.

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Year:  1983        PMID: 6838805      PMCID: PMC1040052          DOI: 10.1136/bjo.67.5.320

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  4 in total

1.  A RARE CONGENITAL ABNORMALITY OF THE EYE.

Authors:  I Mann
Journal:  Br J Ophthalmol       Date:  1930-07       Impact factor: 4.638

2.  Corneal dermoid; report of a case.

Authors:  P N SINHA; S MISHRA
Journal:  Am J Ophthalmol       Date:  1950-07       Impact factor: 5.258

3.  Bilateral corneal dermoids.

Authors:  P Henkind; G Marinoff; A Manas; A Friedman
Journal:  Am J Ophthalmol       Date:  1973-12       Impact factor: 5.258

4.  Corneal transplantation in an infant with corneal dermoid.

Authors:  G W Zaidman; B Johnson; S I Brown
Journal:  Am J Ophthalmol       Date:  1982-01       Impact factor: 5.258

  4 in total
  1 in total

Review 1.  Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes.

Authors:  A M Slavotinek; C J Tifft
Journal:  J Med Genet       Date:  2002-09       Impact factor: 6.318

  1 in total

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