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rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1
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|
pubmed:dateCreated |
2010-2-9
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|
pubmed:abstractText |
In contrast to Autosomal dominant optic atrophy (ADOA), acute loss of vision is normally observed in Leber's hereditary optic neuropathy (LHON) patients. We present a case of a young child with ADOA with a confirmed OPA1 mutation who appeared to have had an acute visual loss in the third year of life.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
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|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
1744-5094
|
|
pubmed:author |
|
|
pubmed:issnType |
Electronic
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|
pubmed:volume |
31
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
44-6
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|
pubmed:meshHeading |
pubmed-meshheading:20141358-Acute Disease,
pubmed-meshheading:20141358-Blindness,
pubmed-meshheading:20141358-Child, Preschool,
pubmed-meshheading:20141358-Electroretinography,
pubmed-meshheading:20141358-Evoked Potentials, Visual,
pubmed-meshheading:20141358-GTP Phosphohydrolases,
pubmed-meshheading:20141358-Humans,
pubmed-meshheading:20141358-Male,
pubmed-meshheading:20141358-Mutation,
pubmed-meshheading:20141358-Optic Atrophy, Autosomal Dominant,
pubmed-meshheading:20141358-Prospective Studies,
pubmed-meshheading:20141358-Visual Acuity
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|
pubmed:year |
2010
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|
pubmed:articleTitle |
Does acute loss of vision in autosomal dominant optic atrophy occur early in childhood?
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|
pubmed:affiliation |
Center for Eye Research Australia, Department of Ophthalmology, University of Melbourne, Melbourne, Australia.
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|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
