Central Cone Dysfunction in Autosomal Dominant Vitreoretino Choroidopathy (ADVIRC)

American Journal of Ophthalmology

Volumn 141, Issue 5, 2006, Pages 940-943

  Oh, Kean T ^a   Vallar, Carrie ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY; CASE REPORT; CENTRAL SCOTOMA; CHORIORETINOPATHY; CLINICAL EXAMINATION; CLINICAL FEATURE; DISEASE ACTIVITY; ELECTROOCULOGRAPHY; ELECTRORETINOGRAPHY; FEMALE; FOLLOW UP; HUMAN; OPHTHALMOSCOPY; OPTICAL COHERENCE TOMOGRAPHY; PRIORITY JOURNAL; RETINA MACULA DEGENERATION; RETINA MACULA LUTEA;

AGED; CHOROID DISEASES; CONES (RETINA); ELECTRORETINOGRAPHY; EYE DISEASES; EYE DISEASES, HEREDITARY; FEMALE; GENES, DOMINANT; HUMANS; PERIMETRY; RETINAL DISEASES; VISION DISORDERS; VISUAL FIELDS; VITREOUS BODY;

EID: 33646205152     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajo.2005.11.041     Document Type: Article

References (5)

1. Kaufman S.J., Goldberg M.F., and Orth D.H. Autosomal dominant vitreoretinochoroidopathy (ADVIRC). Arch Ophthalmol 100 (1982) 272-278
2. Traboulsi E., and Payne W.E. Autosomal dominant vitreoretinochoroidopathy. report of the third family. Arch Ophthalmol 111 (1993) 194-196
3. Han D.P., and Lewandowski M.F. Electro-oculography in autosomal dominant vitreoretinochoroidopathy. Arch Ophthalmol 110 (1992) 1563-1567
4. Kellner U., Jandeck C., Kraus H., and Foerster M.H. Autosomal dominant vitreoretinochoroidopathy with normal electroretinogram in a German family. Graefes Arch Clin Exp Ophthalmol 107 (1998) 816-819
5. Yardley J., Leroy B.P., Hart-Holden N., et al. Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC). Invest Ophthalmol Vis Sci 45 (2004) 3683-3689