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INSIGHTS INTO AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY THROUGH MULTIMODALITY DIAGNOSTIC IMAGING

  • Published:2016-01 Issue:1 Volume:36 Page:119-130
  • ISSN:0275-004X
  • Container-title:Retina
  • language:en
  • Short-container-title:

Author:

Palejwala Neal V.,Gale Michael J.,Clark Rebecca F.,Schlechter Catie,Weleber Richard G.,Pennesi Mark E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference18 articles.

1. Dominantly inherited macular dystrophy with flecks (Stargardt).;Cibis;Arch Ophthalmol,1980

2. . Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to comomasome 6q.;Stone;Arch Ophthalmol,1994

3. . Diverse macular dystrophy phenotype caused by a novel complex mutation in ELOVL4 gene.;Bernstein;Invest Ophthalmol Vis Sci,2001

4. . Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease.;Kniazeva;Ophthalmic Genet,1999

5. . An autosomal dominant bulls-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4.;Michaelides;Invest Ophthalmol Vis Sci,2003

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