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Ophthalmic Paediatrics and Genetics Volume 14, 1993 - Issue 3
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Original Article

Variable Phenotypic Expressivity of Best's Vitelliform Dystrophy

Anat Loewenstein Department of Ophthalmology, Ichilov Hospital, Tel Aviv, Israel
,
Victor Godel Department of Ophthalmology, Ichilov Hospital, Tel Aviv, Israel
,
Li At Godel Department of Ophthalmology, Ichilov Hospital, Tel Aviv, Israel
&
Moshe Lazar Department of Ophthalmology, Ichilov Hospital, Tel Aviv, Israel
Pages 131-136 | Accepted 20 Sep 1993, Published online: 08 Jul 2009

Citations (7)

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Read on this site (1)

Louise Eksandh, Benjamin Bakall, Birgitta Bauer, Claes Wadelius & Sten Andréasson. (2001) Best’s vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene. Ophthalmic Genetics 22:2, pages 107-115.
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Articles from other publishers (6)

A C Cohn, C Turnbull, J B Ruddle, R H Guymer, L S Kearns, S Staffieri, H T Daggett, A W Hewitt & D A Mackey. (2010) Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutations. Eye 25:2, pages 208-217.
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Thomas K.M. Lee, M. Thomas Clandinin, Marc Hébert & Ian M. MacDonald. (2010) Effect of docosahexaenoic acid supplementation on the macular function of patients with Best vitelliform macular dystrophy: randomized clinical trial. Canadian Journal of Ophthalmology 45:5, pages 514-519.
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Camiel J.F. Boon, B. Jeroen Klevering, Bart P. Leroy, Carel B. Hoyng, Jan E.E. Keunen & Anneke I. den Hollander. (2009) The spectrum of ocular phenotypes caused by mutations in the BEST1 gene. Progress in Retinal and Eye Research 28:3, pages 187-205.
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K. Pollack, F. R. Kreuz & L. E. Pillunat. (2005) Morbus Best mit normalem EOGBest’s disease with normal EOG. Der Ophthalmologe 102:9, pages 891-894.
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Kimberly K Reed. (2000) Differential diagnosis of hereditary pigmentary maculopathies. Clinical Eye and Vision Care 12:1-2, pages 3-14.
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Germaine M. Caldwell, Laura E. Kakuk, Irina B. Griesinger, Stacey A. Simpson, Norma J. Nowak, Kent W. Small, Irene H. Maumenee, Philip J. Rosenfeld, Paul A. Sieving, Thomas B. Shows & Radha Ayyagari. (1999) Bestrophin Gene Mutations in Patients with Best Vitelliform Macular Dystrophy. Genomics 58:1, pages 98-101.
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