Please use this identifier to cite or link to this item:
Title: Foveal development and nystagmus.
Authors: Proudlock, F
Gottlob, I
First Published: Sep-2011
Citation: ANN N Y ACAD SCI, 2011, 1233, pp. 292-297
Abstract: The combination of optical coherence tomography (OCT) and genetic methods along with other clinical diagnostic tools permit the discrimination of infantile nystagmus subtypes with a precision that has not previously been possible. Analysis of specific diseases, such as albinism and achromatopsia as well as known genetic abnormalities, such as FRMD7 and PAX6 mutations, shows subtle but significant differences between nystagmus subtypes using eye movement recordings. In addition, OCT can be used to chart the progression of retinal diseases with age, for example, as has been shown in achromatopsia. OCT can also be used to predict the level of visual deficit due to retinal abnormalities, as demonstrated for albinism. These findings suggest that the classification of all infantile nystagmus into one single entity is premature.
DOI Link: 10.1111/j.1749-6632.2011.06174.x
eISSN: 1749-6632
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences

Files in This Item:
There are no files associated with this item.

Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.