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A congenital cataract was discovered, and Styron was discharged from the Marine Corps.
The Arg233Lys AQP0 mutation disturbs aquaporin 0-calmodulin interaction causing polymorphic congenital cataract.
Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract.
Litt, M. et al. Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.
To determine the visual outcome and surgical complication rates of patients with isolated inherited congenital cataract.
Objective: To determine the incidence of the association of rubella virus with congenital cataract.
To evaluate the rate of axial growth after congenital cataract surgery.
Background: The association of rubella virus (RV) with congenital cataract has been well established.
To report the long-term risk of glaucoma development in children following congenital cataract surgery.
To report and compare visual and glaucoma outcomes in primary congenital glaucoma (PCG) vs glaucoma following congenital cataract surgery (GFCS).
To evaluate central corneal thickness (CCT) changes after congenital cataract surgery with or without intraocular lens (IOL) implantation.
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