Abstract
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 language | English (US) |
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Pages (from-to) | 170-172 |
Number of pages | 3 |
Journal | Journal of AAPOS |
Volume | 20 |
Issue number | 2 |
DOIs | |
State | Published - Apr 1 2016 |
Externally published | Yes |
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Ophthalmology