Unilateral glaucoma in Sotos syndrome (cerebral gigantism)

Michael T. Yen, Steven J. Gedde, John T. Flynn

Research output: Contribution to journalArticle

10 Scopus citations

Abstract

PURPOSE: To report a patient with unilateral glaucoma associated with Sotos syndrome. Sotos syndrome (cerebral gigantism) is a disorder of growth and development with characteristic facial changes and normal endocrine function. Ocular manifestations may also include megalocornea, iris hypoplasia, cataracts, megalophthalmos, strabismus, nystagmus, and retinal dystrophy. METHODS: Case report. A 50 year-old man with the clinical features of Sotos syndrome presented with complaints of decreased vision in the left eye. RESULTS: Ophthalmologic examination revealed bilateral megalocornea, megalophthalmos, iris hypoplasia and transillumination defects, cataracts, and unilateral glaucoma. Intraocular pressure was lowered, and visual field loss was stabilized with topical medications. CONCLUSION: Sotos syndrome patients should be examined routinely to allow for early detection and treatment of potential ocular problems, including glaucoma. Copyright (C) 2000 Elsevier Science Inc.

Original languageEnglish (US)
Pages (from-to)851-853
Number of pages3
JournalAmerican journal of ophthalmology
Volume130
Issue number6
DOIs
StatePublished - Dec 1 2000

ASJC Scopus subject areas

  • Ophthalmology

Fingerprint Dive into the research topics of 'Unilateral glaucoma in Sotos syndrome (cerebral gigantism)'. Together they form a unique fingerprint.

  • Cite this