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. 2020 Jun;68(6):1173-1175.
doi: 10.4103/ijo.IJO_1346_19.

Autosomal recessive bestrophinopathy with macular hole

Raj Shri Hirawat  1 , C K Nagesha  2 , Megha M Divakar  2
Affiliations

Autosomal recessive bestrophinopathy with macular hole

Raj Shri Hirawat et al. Indian J Ophthalmol. 2020 Jun.
No abstract available

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Conflict of interest statement

None

Figures

Figure 1
Figure 1
Composite figure showing bilateral subretinal deposits (a and b); full-thickness macular hole in right eye (c) and intraretinal and subretinal fluid collection in left eye (d)
Figure 2
Figure 2
Full flash electroretinogram showing of right and left eye waveforms under light and dark adaptations
Figure 3
Figure 3
Electrooculogram of right and left eye with Arden ratio
See this image and copyright information in PMC

References

    1. Borman AD, Davidson AE, O'Sullivan J, Thompson DA, Robson AG, De Baere E, et al. Childhood-onset autosomal recessive bestrophinopathy. Arch Ophthalmol. 2011;129:1088–93. - PubMed
    1. Boon CJ, van den Born LI, Visser L, Keunen JE, Bergen AA, Booij JC, et al. Autosomal recessive bestrophinopathy: Differential diagnosis and treatment options. Ophthalmology. 2013;120:809–20. - PubMed
    1. Nakanishi A, Ueno S, Hayashi T, Katagiri S, Kominami T, Ito Y, et al. Clinical and genetic findings of autosomal recessive bestrophinopathy in Japanese cohort. Am J Ophthalmol. 2016;168:86–94. - PubMed

MeSH terms

Supplementary concepts