Source:http://linkedlifedata.com/resource/pubmed/id/11227385
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2001-2-28
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pubmed:abstractText |
Pigment dispersion syndrome affects up to 4% of the white population. It is characterized by the presence of transillumination defects, Krukenberg's spindle and dense trabecular meshwork pigmentation. Open-angle glaucoma will develop in as many as 50% of affected patients. In this study we describe the familial occurrence of pigment dispersion syndrome in six North American pedigrees and the phenotypic characteristics with respect to pigment dispersion syndrome and glaucoma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0008-4182
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
36
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
11-7
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:11227385-Adult,
pubmed-meshheading:11227385-Aged,
pubmed-meshheading:11227385-Exfoliation Syndrome,
pubmed-meshheading:11227385-Female,
pubmed-meshheading:11227385-Genes, Dominant,
pubmed-meshheading:11227385-Glaucoma, Open-Angle,
pubmed-meshheading:11227385-Humans,
pubmed-meshheading:11227385-Male,
pubmed-meshheading:11227385-Middle Aged,
pubmed-meshheading:11227385-Pedigree,
pubmed-meshheading:11227385-Phenotype
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pubmed:year |
2001
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pubmed:articleTitle |
Familial occurrence of pigment dispersion syndrome.
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pubmed:affiliation |
University of Ottawa Eye Institute, Ottawa Hospital, Ottawa, Ont.
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pubmed:publicationType |
Journal Article
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