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Low vision assessment and management in Stargardt disease: diagnostic approach and therapeutic strategies. Case report

https://doi.org/10.21516/2072-0076-2026-19-2-177-181

Abstract

A 19-year-old female presented to the outpatient department with reduced visual acuity and recurrent headaches. Initially recorded as 15 due to an oversight, her age was clarified, and her best-corrected visual acuity was measured at 6/60P logMAR bilaterally, with a prescription of -0.5 D. Cyclorefraction revealed -1.5 D bilaterally. Fundus examination demonstrated vascular tortuosity, bull’s-eye maculopathy, and peripheral pigmentary retinopathy, leading to a diagnosis of Stargardt disease, confirmed through advanced imaging. She was referred to the low vision department for a specialized assessment to address her progressive vision loss and was also evaluated by neurology for recurrent headaches. A comprehensive low vision evaluation helped determine her specific visual needs, with recommendations aimed at enhancing her daily activities and managing her visual prognosis. This case underscores the essential role of low vision assessments in juvenile macular dystrophies like Stargardt disease, where early intervention and personalized visual aids can significantly improve functional vision and quality of life.

About the Authors

R. Faheem
Pakistan Institute of Ophthalmology, Al-Shifa Trust Eye Hospital
Pakistan

Rabia Faheem — Optometrist.

Rawalpindi, 4600



M. Saad
Lincoln University College, Wisma Lincoln
Malaysia

Muhammad Saad — Dr. of Medicine, fellow, Ophthalmology Department.

4730, Petaling Jaya, Selangor Darul Ehsan



S. Ullah
Pakistan Institute of Ophthalmology, Al-Shifa Trust Eye Hospital; Lincoln University College, Wisma Lincoln
Pakistan

Saif Ullah — PhD Scholar, Pakistan Institute of Ophthalmology, Al-Shifa Trust Eye Hospital; assistant professor, department of Health Sciences, Lincoln University College, Wisma Lincoln.

Rawalpindi, 4600, Pakistan; 4730, Petaling Jaya, Selangor Darul Ehsan, Malaysia



M. Noor
Pakistan Institute of Ophthalmology, Al-Shifa Trust Eye Hospital
Pakistan

Muqaddas Noor — B.Sc. Honor Optometry.

Rawalpindi, 4600



I. Nasim
Pakistan Institute of Ophthalmology, Al-Shifa Trust Eye Hospital
Pakistan

Iffat Nasim — B.Sc. Honor Optometry and Orthoptics, Optometrist.

Rawalpindi, 4600



References

1. Dandona L, Dandona R. Revision of visual impairment definitions in the International Statistical Classification of Diseases. BMC Med. 2006 Mar 16; 4: 7. doi: 10.1186/1741-7015-4-7

2. Westerfeld C, Mukai S. Stargardt’s disease and the ABCR gene. Semin Ophthalmol. 2008 Jan-Feb; 23 (1): 59–65. doi: 10.1080/08820530701745249

3. Al-Khuzaei S, Broadgate S, Foster CR, et al. An overview of the genetics of ABCA4 retinopathies, an evolving story. Genes (Basel). 2021 Aug 13; 12 (8): 1241. doi: 10.3390/genes12081241

4. Fishman GA. Fundus flavimaculatus. A clinical classification. Arch Ophthalmol. 1976 Dec; 94 (12): 2061–7. doi: 10.1001/archopht.1976.03910040721003

5. Huang D, Heath Jeffery RC, Aung-Htut MT, et al. Stargardt disease and progress in therapeutic strategies. Ophthalmic Genet. 2022 Feb; 43 (1): 1–26. doi: 10.1080/13816810.2021.1966053

6. Maguire AM, Bennett J, Aleman EM, Leroy BP, Aleman TS. Clinical perspective: Treating RPE65-associated retinal dystrophy. Mol Ther. 2021 Feb 3; 29 (2): 442–63. doi: 10.1016/j.ymthe.2020.11.029

7. Fujinami K, Waheed N, Laich Y, et al. Stargardt macular dystrophy and therapeutic approaches. Br J Ophthalmol. 2024 Mar 20; 108 (4): 495–505. doi: 10.1136/bjo-2022-323071

8. Ghenciu LA, Ha egan OA, Stoicescu ER, Iacob R, i u AM. Emerging therapeutic approaches and genetic insights in Stargardt disease: A comprehensive review. Int J Mol Sci. 2024 Aug 14; 25 (16): 8859. doi: 10.3390/ijms25168859

9. Abalem MF, Otte B, Andrews C, et al. Peripheral visual fields in ABCA4 Stargardt disease and correlation with disease extent on ultra-widefield fundus autofluorescence. Am J Ophthalmol. 2017 Dec; 184: 181–8. doi: 10.1016/j.ajo.2017.10.006

10. Sofi F, Sodi A, Franco F, et al. Dietary profile of patients with Stargardt’s disease and Retinitis Pigmentosa: is there a role for a nutritional approach? BMC Ophthalmol. 2016 Jan 22; 16: 13. doi: 10.1186/s12886-016-0187-3

11. Rahman N, Georgiou M, Khan KN, Michaelides M. Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic options. Br J Ophthalmol. 2020 Apr; 104 (4): 451–60. doi: 10.1136/bjophthalmol-2019-315086


Review

For citations:


Faheem R., Saad M., Ullah S., Noor M., Nasim I. Low vision assessment and management in Stargardt disease: diagnostic approach and therapeutic strategies. Case report. Russian Ophthalmological Journal. 2026;19(2):177-181. https://doi.org/10.21516/2072-0076-2026-19-2-177-181

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ISSN 2072-0076 (Print)
ISSN 2587-5760 (Online)