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Fig. 4 | BMC Ophthalmology

Fig. 4

From: A novel missense variant expands the phenotype and genotype of PAX6-associated foveal hypoplasia accompanied by various manifestations of anterior segment dysgenesis

Fig. 4

Anterior segments of the twin-boy. (Left column for the right eye and right column for the left eye.)

A-B. Corneal diameters were 10 mm and 9 mm in the horizontal and vertical meridians, respectively, and sclerocornea was presented. Both of the pupils were almost oval but displaced superiorly and nasally. C-D. Both pupils were relatively poorly dilated and threadlike persistent membrane was presented only at 12 o’clock in the left eye. E-F. The reflection of the posterior capsule of the left lens was higher than normal with side light by slit-lamp biomicroscopy. G-H. Anterior OCT showed pupillary displacement and abnormal tissue membrane climbing from the root of iris to the corneal endothelium of anterior chamber angle

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