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Autosomal dominant optic atrophy. A spectrum of disability.

Authors: C S, Hoyt;

Autosomal dominant optic atrophy. A spectrum of disability.

Abstract

Autosomal dominant optic atrophy is an abiotrophy with an insidious onset in the first decade of life. The clinical features of 31 individuals in six pedigrees are detailed in this study. These data suggest that here is considerable intrafamilial and interfamilial expression of dysfunction. Moreover, asymmetry of the visual loss in not unusual. An unexpected result of this study is the previously unreported frequent association of a neural hearing loss with this disorder.

Keywords

Adult, Male, Color Perception Tests, Adolescent, Hearing Loss, Sensorineural, Visual Acuity, Infant, Middle Aged, Nystagmus, Pathologic, Optic Atrophy, Child, Preschool, Humans, Visual Fields, Child, Aged, Genes, Dominant

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Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
130
Top 10%
Top 1%
Average
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