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Fig. 7 | BMC Ophthalmology

Fig. 7

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

Fig. 7

Posterior segments of the mother. (Left column for the right eye and right column for the left eye.)

A-B. Optical coherence tomography of the macula. Both eyes exhibited grade 3 FH with only ONL widening, foveal retinal thickness measuring 320 μm and 304 μm respectively. C-F. Bilateral opacity of the vitreous and cupping of the left optic nerve head (cup/disc ratio about 0.5) was presented. The trunk of nasal retinal vein divided into upper and lower branches only after crossing the edge of optic disc. G-H. Ophthalmic ultrasound showed bilateral vitreous opacity and the axial length was 21.9 mm (right eye) and 21.8 mm (left eye). No space-occupying lesions or retinal detachment was observed

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BMC Ophthalmology

ISSN: 1471-2415

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