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Fig. 2 | BMC Ophthalmology

Fig. 2

From: A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family

Fig. 2

Fundus photograph and OCT images of the proband. A Colour fundus photographs of the proband revealed widespread macular atrophy, narrow vessels, optic disc pallor, and early pigmentary bone spicules. B OCT of the proband showing significantly reduced retinal thickness, and inner segment/outer segment (IS/OS) are not visualized in some parts of the retina

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BMC Ophthalmology

ISSN: 1471-2415

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