Ophthalmic features of Alagille syndrome (Arteriohepatic dysplasia)

K. K. Wells, J. S. Pulido, G. F. Judisch, K. C. Ossoinig, T. C. Fisher, D. R. LaBrecque

Research output: Contribution to journalArticle

24 Scopus citations

Abstract

Eight patients with Alagille syndrome (AGS) are reported. In addition to previously reported findings of posterior embryotoxon, pigmentary retinopathy, and choroidal folds, new findings include decreased axial eye lengths, small corneal diameters, and shallow anterior chambers. Optic disc swelling was noted ophthalmoscopically and abnormally increased orbital subarachnoidal fluid was detected through measurements of the arachnoidal diameters with standardized echography.

Original languageEnglish (US)
Pages (from-to)130-135
Number of pages6
JournalJournal of pediatric ophthalmology and strabismus
Volume30
Issue number2
StatePublished - Jan 1 1993

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Ophthalmology

Fingerprint Dive into the research topics of 'Ophthalmic features of Alagille syndrome (Arteriohepatic dysplasia)'. Together they form a unique fingerprint.

  • Cite this

    Wells, K. K., Pulido, J. S., Judisch, G. F., Ossoinig, K. C., Fisher, T. C., & LaBrecque, D. R. (1993). Ophthalmic features of Alagille syndrome (Arteriohepatic dysplasia). Journal of pediatric ophthalmology and strabismus, 30(2), 130-135.