Infantile-onset glaucoma and anterior megalophthalmos in osteogenesis imperfecta

Brenda L. Bohnsack*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


Osteogenesis imperfecta (OI) is an inherited condition in which defects in type 1 collagen cause abnormalities in many tissues and organs, including bone, teeth, heart valves, and eyes. We describe a 6-month-old boy with OI who presented with anterior megalophthalmos of the right eye and infantile-onset glaucoma of the left eye. To our knowledge, this is the first reported case of these types of congenital eye anomalies in an infant with OI.

Original languageEnglish (US)
Pages (from-to)170-172
Number of pages3
JournalJournal of AAPOS
Issue number2
StatePublished - Apr 1 2016
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Ophthalmology


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