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Fig. 3 | BMC Ophthalmology

Fig. 3

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

Fig. 3

Posterior segments of the twin-girl. (Left column for the right eye and right column for the left eye.)

A-B. Optical coherence tomography of the macula. The right eye exhibited grade 1 FH with a shallow foveal pit measuring 261 μm of retinal thickness, presence of ONL widening, and presence of OS lengthening, and the left eye demonstrated grade 4 FH with absence of foveal pit, ONL widening, and OS lengthening. C-F. The optic discs demonstrated normal size and colour, and the trunk of nasal retinal vein divided into upper and lower branches only after crossing the edge of optic disc. G-H. The axial length was 21.3 mm (right eye) and 21.1 mm (left eye) with no space-occupying lesions, vitreous opacity or retinal detachment

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BMC Ophthalmology

ISSN: 1471-2415

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