Fine central macular dots associated with childhood-onset Stargardt Disease

Acta Ophthalmol. 2014 Mar;92(2):e157-9. doi: 10.1111/aos.12259. Epub 2013 Sep 11.

Authors

Kaoru Fujinami¹, Ravjit Singh, Joseph Carroll, Jana Zernant, Rando Allikmets, Michel Michaelides, Anthony T Moore

Affiliation

¹ Moorfields Eye Hospital, London, UK; UCL Institute of Ophthalmology, London, UK; National Institute of Sensory Organs, National Hospital Organization, National Tokyo Medical Center, Tokyo, Japan; Department of Ophthalmology, School of Medicine, Keio University, Tokyo, Japan.

PMID: 24020726
DOI: 10.1111/aos.12259

No abstract available

Publication types

Case Reports
Letter

MeSH terms

ATP-Binding Cassette Transporters / genetics
Child
Consanguinity
DNA Mutational Analysis
Female
Fluorescein Angiography
Humans
Macular Degeneration / complications
Macular Degeneration / diagnosis
Macular Degeneration / genetics
Mutation / genetics
Retinal Diseases / diagnosis
Retinal Diseases / etiology*
Retinal Diseases / genetics
Siblings
Stargardt Disease
Tomography, Optical Coherence
Visual Acuity / physiology

Substances

ABCA4 protein, human
ATP-Binding Cassette Transporters