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Stargardt Disease

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Manual of Retinal Diseases

Abstract

Stargardt Disease is the most common juvenile-onset macular dystrophy

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References and Suggested Reading

  1. Abdollahi SH, Hirose T. Stargardt-Fundus flavimaculatus: recent advancements and treatment. Semin Ophthalmol. 2013;28(5–6):372–6.

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  2. Koenekoop RK, Lopez I, den Hollander AI, Allikmets R, Cremers FPM. Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas, and solutions. Clin Exp Ophthalmol. 2007;35:473–85.

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  3. Lois N, Holder GE, Bunce C, Fitzke FW, Bird AC. Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus. Arch Ophthalmol. 2001;119:359–69.

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  4. Rotenstreich Y, Fishman GA, Anderson RJ. Visual acuity loss and clinical observations in a large series of patients with Stargardt disease. Ophthalmology. 2003;110(6):1151–8.

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  5. Walia S, Fishman GA. Natural history of phenotypic changes in Stargardt macular dystrophy. Ophthalmic Genet. 2009;30:63–8.

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Correspondence to Veeral S. Shah MD, PhD .

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© 2016 Springer International Publishing Switzerland

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Rahman, S.A., Shah, V.S. (2016). Stargardt Disease. In: Medina, C., Townsend, J., Singh, A. (eds) Manual of Retinal Diseases. Springer, Cham. https://doi.org/10.1007/978-3-319-20460-4_21

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  • DOI: https://doi.org/10.1007/978-3-319-20460-4_21

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-20459-8

  • Online ISBN: 978-3-319-20460-4

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