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rdf:type |
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lifeskim:mentions |
|
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pubmed:issue |
6
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pubmed:dateCreated |
2007-12-25
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pubmed:abstractText |
Ehlers-Danlos syndrome (EDS) is a hereditary connective tissue disorder caused by defective collagen synthesis and categorized into 11 types based on genetic mutations and clinical features.(1) Its principal clinical characteristics include hyperelasticity and vulnerability of the skin and joints to laxity, and fragility of blood vessels.
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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:issn |
0021-5155
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pubmed:author |
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pubmed:copyrightInfo |
(c) Japanese Ophthalmological Society 2007
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pubmed:issnType |
Print
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
453-5
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pubmed:meshHeading |
pubmed-meshheading:18158597-Artificial Organs,
pubmed-meshheading:18158597-Child,
pubmed-meshheading:18158597-Cornea,
pubmed-meshheading:18158597-Corneal Opacity,
pubmed-meshheading:18158597-Corneal Transplantation,
pubmed-meshheading:18158597-Ehlers-Danlos Syndrome,
pubmed-meshheading:18158597-Humans,
pubmed-meshheading:18158597-Male,
pubmed-meshheading:18158597-Retinal Detachment,
pubmed-meshheading:18158597-Retinal Vessels,
pubmed-meshheading:18158597-Transplantation, Homologous,
pubmed-meshheading:18158597-Visual Acuity,
pubmed-meshheading:18158597-Vitrectomy,
pubmed-meshheading:18158597-Vitreous Detachment,
pubmed-meshheading:18158597-Vitreous Hemorrhage
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pubmed:articleTitle |
Abnormal retinal blood vessels in Ehlers-Danlos syndrome type VI.
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pubmed:affiliation |
Department of Ophthalmology, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan. chikamot@yamaguchi-u.ac.jp
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pubmed:publicationType |
Journal Article,
Case Reports
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