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Ronzina I.A.

Research Institute of Eye Diseases

Sheremet N.L.

Krasnov Research Institute of Eye Diseases

Zhorzholadze N.V.

Research Institute of Eye Diseases

Asymmetric form of pigmentary retinopathy (case study)

Authors:

Ronzina I.A., Sheremet N.L., Zhorzholadze N.V.

More about the authors

Journal: Russian Annals of Ophthalmology. 2021;137(5): 114‑121

DOI: 10.17116/oftalma2021137051114

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Table of contents

ASYMMETRIC FORM OF PIGMENTARY RETINOPATHY (CASE STUDY)
ASYMMETRIC FORM OF PIGMENTARY RETINOPATHY (CASE STUDY)

To cite this article:

Ronzina IA, Sheremet NL, Zhorzholadze NV. Asymmetric form of pigmentary retinopathy (case study). Russian Annals of Ophthalmology. 2021;137(5):114‑121. (In Russ.)
https://doi.org/10.17116/oftalma2021137051114

Подписка 2025-2 (Russian Annals of Ophthalmology)
 
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Unilateral pigmentary retinopathy (PR) is a rare, atypical form of hereditary retinal pathology. Different types of secondary retinopathy associated with various non-hereditary diseases, trauma or intoxication can imitate unilateral PR. Therefore, it is important to determine the cause of visual disorders and differentiate between unilateral and asymmetric PR. The article presents an example of using modern structural and functional diagnostic methods that helped diagnose the asymmetric form of the disease in a patient with suspected unilateral PR.

Keywords:

asymmetric pigmentary retinopathy
autofluorescence
optical coherence tomography
electroretinography

Authors:

Ronzina I.A.

Research Institute of Eye Diseases

Sheremet N.L.

Krasnov Research Institute of Eye Diseases

Zhorzholadze N.V.

Research Institute of Eye Diseases

Received:

30.11.2020

Accepted:

13.01.2021

List of references:

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  4. Marsiglia M, Duncker T, Peiretti E, Brodie SE, Tsang SH. Unilateral retinitis pigmentosa: a proposal of genet ic pathogenic mechanisms. Eur J Ophthalmol. 2012;22:654-660.  https://doi.org/10.5301/ejo.5000086
  5. Mukhopadhyay R, Holder GE, Moore AT, Webster AR. Unilateral retinitis pigmentosa occurring in an individual with a germline mutation in the RP1 gene. Arch Ophthalmol. 2011;129:954-956.  https://doi.org/10.1001/archophthalmol.2011.171
  6. Rogatina EV, Zol’nikova IV. Unilateral retinitis pigmentosa associated with congenital heart disease. Vestnik oftal’mologii. 2005;(2):52-54. (In Russ.).
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  14. Francois J, Verriest G. Retinopathie pigmentaire unilaterale. Int J Ophthalmol. 1952;124:65-88.  https://doi.org/10.1159/000301252
  15. Zolnikova IV, Milash SV, Chernyak AB, Egorova IV, Rogatina EV, Eremeeva EA, Rogova SYu. Thickness of the retinal photoreceptor layers and the choroid, and bioelectrical activity of the macula in retinitis pigmentosa. Vestnik oftal’mologii. 2019;(3):39-45. (In Russ.). https://doi.org/10.17116/oftalma201913503139
  16. Dediashvili NG, Sheludchenko VM. Spectral correction of vision and electrophysiological measurements of the eye. Vestnik oftal’mologii. 2018;134(5-2):231-237. (In Russ.). https://doi.org/10.17116/oftalma2018134052231
  17. Shpak AA, Shkvorchenko DO, Vedernikova OYu, Shahabutdinova PM. Natural course of lamellar macular holes. Vestnik oftal’mologii. 2020;136(4):5-10. (In Russ.). https://doi.org/10.17116/oftalma20201360415

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