HEREDITARY MACULAR DYSTROPHIES. PART 1. DYSTROPHIES ASSOCIATED WITH DYSFUNCTION OF RETINAL PIGMENT EPITHELIAL CELLS
- Authors: Katargina L.A1, Denisova E.V1, Osipova N.A.1
-
Affiliations:
- The Helmholtz Moscow Research Institute of Eye Diseases of Russian Ministry of Health
- Issue: Vol 13, No 2 (2018)
- Pages: 103-108
- Section: Articles
- URL: https://bakhtiniada.ru/1993-1859/article/view/39603
- DOI: https://doi.org/10.18821/1993-1859-2018-13-2-103-108
- ID: 39603
Cite item
Full Text
Abstract
Full Text
##article.viewOnOriginalSite##About the authors
L. A Katargina
The Helmholtz Moscow Research Institute of Eye Diseases of Russian Ministry of HealthMoscow, 105062, Russian Federation
E. V Denisova
The Helmholtz Moscow Research Institute of Eye Diseases of Russian Ministry of HealthMoscow, 105062, Russian Federation
Natal’ja A. Osipova
The Helmholtz Moscow Research Institute of Eye Diseases of Russian Ministry of Health
Email: natashamma@mail.ru
ophthalmologist of ophthalmology department (pediatric surgery) of The Helmholtz Moscow Research Institute of Eye Diseases of the Ministry of Health of the Russian Federation Moscow, 105062, Russian Federation
References
- Stargardt K. Uber familiare, progressive degenerationin der makulagegend des auges. Graefes Arch. Clin. Exp. Ophthalmol. 1909; 71: 534-50.
- Шамшинова А.М. Наследственные и врожденные заболевания сетчатки и зрительного нерва. М.: Медицина, 2001.
- Allikmets R., Singh N., Sun H., Shroyer N.F., Hutchinson A. et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat. Genet. 1997; 15: 236-46.
- Шамшинова А.М., Зольникова И.В. Молекулярно-генетические основы патогенеза наследственных дистрофий сетчатки. Медицинская генетика. 2004; 4: 160-9.
- Zolnikova I.V., Rogatina E.V., Egorova I.V., Levina D.V., Demenkova O.N., Strelnikov V.V., Tanas A.S., Skvortsova N.A., Barh D., Prikaziuk E.G., Ivanova M.E. Stargardt disease-associated mutation spectrum of a Russian federation cohort. European Journal of Medical Genetics. 2017; 60(2): 140-7.
- Зольникова И.В., Рогатина Е.В. Дистрофия Штаргардта: клиника, диагностика, патогенез, лечение. Клиницист. 2010; 1: 29-33.
- Franceschetti A., Francois J. Fundus flavimaculatus. Arch. d’Ophthalmol. 1965; 25: 505-30.
- Delori F.C., Staurenghi G., Arend O., Dorey K., Goger D.G., Weiter J.J. In vivo measurements of lipofuscin in Stargardt’s disease - fundus flavimaculatus. Invest. Ophthalmol. Vis. Sci. 1995; 36: 2327-31.
- Fishman G.A., Farber M., et al. Visual acuity loss in patients with Stargardt’s macular dystrophy. Ophthalmology. 1987; 94: 809-14.
- Зольникова И.В., Карлова И.З., Рогатина Е.В. Макулярная и мультифокальная электроретинография в диагностике дистрофии Штаргардта. Вест. офтальмол. 2009; 1(125): 41-6.
- Berson E.L. Retinitis pigmentosa. Invest. Ophthalmol. Vis. Sci. 1993; 34(5): 1659-76.
- Greenstein V.C., Nunez J., Lee W., Schuerch K. et al. A comparison of en face optical coherence tomography and fundus autofluorescence in Stargardt disease. Invest. Ophthalmol. Vis. Sci. 2017; 58 (12): 5227-36.
- Best F. Ueber eine hereditare maculaaffektion. Z. Augenheklkd. 1905; 13: 199-212.
- Marmorstein A.D., Kinnick T.R., Stanton J.B., Johnson A.A, Lynch R.M., Marmorstein L.Y. Bestrophin-1 influences transepithelial electrical properties and Ca2+ signaling in human retinal pigment epithelium. Molecular Vision. 2015; 21: 347-59.
- Зольникова И.В., Рогатина Е.В., Орловская Л.С., Пономарева Е.Н. Мультифокальная, макулярная и паттерн-ЭРГ при вителлиформной макулодистофии Беста. Офтальмология. 2006; 3(2): 29-36.
- Katargina L., Denisova E., Kogoleva L., Novikova O., Osipova N. Choroidal neovascularization secondary to best viteliform macular dystrophy: is it rare? Eur. J. Ophthalmol. 2017; 27 (5): Abstracts from the 43 EPOS Annual Meeting, 31 August-2 September 2017. - Oxford, UK. - P. e157.
Supplementary files
