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Infantile-onset glaucoma and anterior megalophthalmos in osteogenesis imperfecta
1Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor.
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.
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