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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2004-4-20
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pubmed:abstractText |
Although cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is considered a cerebrovascular disorder with almost exclusively neurological symptoms, the arteriopathy is generalized and involves choroidal and retinal vasculature as demonstrated by fluorescein angiographic and ocular electrophysiological abnormalities. The occurrence of acute visual loss due to nonarteritic anterior ischemic optic neuropathy (NAION) has not previously been reported in CADASIL.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0003-9942
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
61
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
577-80
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15096408-Blindness,
pubmed-meshheading:15096408-Chromosomes, Human, Pair 19,
pubmed-meshheading:15096408-DNA Mutational Analysis,
pubmed-meshheading:15096408-Dementia, Multi-Infarct,
pubmed-meshheading:15096408-Disease Progression,
pubmed-meshheading:15096408-Evoked Potentials, Visual,
pubmed-meshheading:15096408-Exons,
pubmed-meshheading:15096408-Fluorescein Angiography,
pubmed-meshheading:15096408-Functional Laterality,
pubmed-meshheading:15096408-Genetic Predisposition to Disease,
pubmed-meshheading:15096408-Heterozygote Detection,
pubmed-meshheading:15096408-Humans,
pubmed-meshheading:15096408-Magnetic Resonance Imaging,
pubmed-meshheading:15096408-Male,
pubmed-meshheading:15096408-Middle Aged,
pubmed-meshheading:15096408-Optic Atrophy,
pubmed-meshheading:15096408-Optic Neuropathy, Ischemic,
pubmed-meshheading:15096408-Phenotype,
pubmed-meshheading:15096408-Proto-Oncogene Proteins,
pubmed-meshheading:15096408-Receptors, Cell Surface,
pubmed-meshheading:15096408-Receptors, Notch,
pubmed-meshheading:15096408-Visual Cortex
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pubmed:year |
2004
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pubmed:articleTitle |
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
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pubmed:affiliation |
Neurology and Neurometabolic Disease Unit, Center for the Diagnosis, Prevention, and Therapy of Neurological Handicap, Department of Behavioral and Neurological Sciences, University of Siena Medical School, Siena, Italy.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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