 |
 |

Electro-oculography in Autosomal Dominant Vitreoretinochoroidopathy
Dennis P. Han, MD;
Michael F. Lewandowski, RDMS
Arch Ophthalmol. 1992;110(11):1563-1567.
Abstract
Thirteen members of a family presumed to be harboring the gene for autosomal dominant vitreoretinochoroidopathy were examined. In four affected members, electro-oculography demonstrated marked reduction of the Arden ratio (range, 1.1 to 1.5; normal, 1.8), despite electroretinographic evidence of mildly affected rod function and normal cone function. These findings suggested that a diffuse disturbance of the photoreceptor-pigment epithelium complex may have been present prior to widespread loss of photoreceptor function in the affected members of this family. As in previously described families, the pattern of inheritance appeared consistent with autosomal dominance.
Author Affiliations
From the Department of Ophthalmology, Medical College of Wisconsin, Milwaukee.
Footnotes
Accepted for publication April 2, 1992.
Reprint requests to Eye Institute, 8700 W Wisconsin Ave, Milwaukee, WI 53226 (Dr Han).
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
Molecular Physiology of Bestrophins: Multifunctional Membrane Proteins Linked to Best Disease and Other Retinopathies
Hartzell et al.
Physiol. Rev. 2008;88:639-672.
ABSTRACT
| FULL TEXT
The Light Peak of the Electroretinogram Is Dependent on Voltage-gated Calcium Channels and Antagonized by Bestrophin (Best-1)
Marmorstein et al.
JGP 2006;127:577-589.
ABSTRACT
| FULL TEXT
Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC)
Yardley et al.
IOVS 2004;45:3683-3689.
ABSTRACT
| FULL TEXT
Histopathologic Study of Autosomal Dominant Vitreoretinochoroidopathy in a 26-Year-Old Woman
Han et al.
Arch Ophthalmol 1995;113:1561-1566.
ABSTRACT
|