Literature DB >> 868964

Iris transillumination and variable expression in ectopia lentis et pupillae.

J A Luebbers, M F Goldberg, R Herbst, J Hattenhauer, A E Maumenee.   

Abstract

Six children in three families showed variations of the rare genetic syndrome, ectopia lentis et pupillae. The siblings in two affected families demonstrated intermingling of simple lens ectopia with ectopia lentis et pupillae, suggesting that some types of simple ectopia lentis represent an incompletely expressed form of the full ectopia lentis et pupillae syndrome. Those patients with simple lens ectopia as well as those with ectopic lenses and pupils had striking transillumination of the iris periphery. Microphakia, cataract, and other anterior segment abnormalities were also observed.

Entities:  

Mesh:

Year:  1977        PMID: 868964     DOI: 10.1016/0002-9394(77)90130-1

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


  4 in total

1.  Ectopia lentis et pupillae: report of a unilateral case and surgical management.

Authors:  Panagiotis Ekonomidis; Sofia Androudi; Periklis Brazitikos; Alexandros Alexandridis
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2005-11-29       Impact factor: 3.117

2.  Megalocornea. Clinical and genetic aspects.

Authors:  F M Meire
Journal:  Doc Ophthalmol       Date:  1994       Impact factor: 2.379

Review 3.  Ectopia lentis et pupillae syndrome in three generations.

Authors:  J R Cruysberg; A Pinckers
Journal:  Br J Ophthalmol       Date:  1995-02       Impact factor: 4.638

4.  Clinical manifestations of ectopia lentis et pupillae in 16 patients.

Authors:  M F Goldberg
Journal:  Trans Am Ophthalmol Soc       Date:  1988
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.