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Methods: Seventy-six patients with different forms of anterior segment dysgenesis were classified clinically.
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Five of these six patients were examined and all demonstrated anterior segment anomalies.
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Purpose: Mutations of the forkhead transcription factor gene FOXC1 result in anterior segment anomalies.
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Adult chimeric eyes displayed a range of defects including anterior segment dysgenesis and cataracts.
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The clinical and demographic characteristics, laser parameters, anterior segment complications, and structural outcomes were evaluated.
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However, there are reports of severe congestion in the anterior segment of the graft after transplantation.
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In some clinical and experimental cases, the anterior segment appeared entirely normal despite a posterior rupture.
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Graft survival and visual outcome are best in patients with trauma limited to the anterior segment.
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UG patients exhibited significant decreases in mean cell score of the anterior segment after ripasudil treatment.
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Cataract was the most common anterior segment complication.
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The anatomic structures of the anterior segment were monitored by AS-OCT before and after the treatment.
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Her best-corrected visual acuity, color vision, intraocular pressures, and anterior segment examination findings were normal bilaterally.
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Ultrasound biomicroscopy is a promising procedure for examining the anterior segment of eyes with corneal opacity.
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In the rat anterior segment, the highest cystatin C concentrations were found in the ciliary epithelium.
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The gene encodes a transcription factor which has a key role in lens and anterior segment development.
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The anterior segment examination shows no peculiarities.
