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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 |
1977-7-23
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pubmed:abstractText |
A 57-year-old black man had François-Neetens speckled dystrophy of the cornea and orbital phycomycosis. Examination of family members confirmed an auto-somal-dominant pattern of inheritance. Light and electron microscopic study of the cornea of a blind eye disclosed that the corneal opacities were represented by swollen, vacuolated keratocytes filled with histochemically demonstrable acid mucopolysaccharide and complex lipids. Thus, this dystrophy may represent a dominantly inherited metabolic disorder confined to the cornea.
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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 |
0002-9394
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
554-60
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:141212-Adolescent,
pubmed-meshheading:141212-Adult,
pubmed-meshheading:141212-Aged,
pubmed-meshheading:141212-Cornea,
pubmed-meshheading:141212-Corneal Dystrophies, Hereditary,
pubmed-meshheading:141212-Corneal Opacity,
pubmed-meshheading:141212-Epithelial Cells,
pubmed-meshheading:141212-Epithelium,
pubmed-meshheading:141212-Female,
pubmed-meshheading:141212-Genes, Dominant,
pubmed-meshheading:141212-Glycosaminoglycans,
pubmed-meshheading:141212-Histocytochemistry,
pubmed-meshheading:141212-Humans,
pubmed-meshheading:141212-Lipids,
pubmed-meshheading:141212-Male,
pubmed-meshheading:141212-Middle Aged,
pubmed-meshheading:141212-Mucopolysaccharidoses,
pubmed-meshheading:141212-Pedigree
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pubmed:year |
1977
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pubmed:articleTitle |
A clinical and histopathological study of François-Neetens speckled corneal dystrophy.
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pubmed:publicationType |
Journal Article,
Case Reports
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