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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
7
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pubmed:dateCreated |
2001-6-26
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pubmed:abstractText |
Congenital fibrosis of the extraocular muscles (CFEOM) is a rare condition that has been traditionally regarded as a primary eye muscle disease. Recent studies, however, suggest that CFEOM may be the result of a primary neuropathy with secondary myopathic changes.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0161-6420
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
108
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1313-22
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:11425694-Abnormalities, Multiple,
pubmed-meshheading:11425694-Adult,
pubmed-meshheading:11425694-Basal Ganglia,
pubmed-meshheading:11425694-Blepharoptosis,
pubmed-meshheading:11425694-Cerebral Cortex,
pubmed-meshheading:11425694-Child,
pubmed-meshheading:11425694-Child, Preschool,
pubmed-meshheading:11425694-Chromosome Aberrations,
pubmed-meshheading:11425694-Chromosomes, Human, Pair 12,
pubmed-meshheading:11425694-Eye Abnormalities,
pubmed-meshheading:11425694-Eye Movements,
pubmed-meshheading:11425694-Female,
pubmed-meshheading:11425694-Fibrosis,
pubmed-meshheading:11425694-Genetic Linkage,
pubmed-meshheading:11425694-Humans,
pubmed-meshheading:11425694-Lod Score,
pubmed-meshheading:11425694-Magnetic Resonance Imaging,
pubmed-meshheading:11425694-Oculomotor Muscles,
pubmed-meshheading:11425694-Ophthalmoplegia,
pubmed-meshheading:11425694-Pedigree
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pubmed:year |
2001
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pubmed:articleTitle |
Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia.
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pubmed:affiliation |
Department of Ophthalmology, New Children's Hospital, Westmead, Sydney, Australia.
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pubmed:publicationType |
Journal Article,
Case Reports
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