Source:http://linkedlifedata.com/resource/pubmed/id/16906471
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2006-9-14
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pubmed:abstractText |
A patient with early bilateral nuclear cataracts and subsequent diagnosis of Fanconi-Bickel syndrome is described. Despite impaired galactose and glucose metabolism, cataracts have been reported in only few cases with this disorder. We conclude that Fanconi-Bickel syndrome should be considered in the differential diagnosis of neonatal cataracts. The pathogenesis of this complication has not been fully elucidated.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0141-8955
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
685
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pubmed:dateRevised |
2007-3-21
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pubmed:meshHeading | |
pubmed:year |
2006
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pubmed:articleTitle |
Bilateral nuclear cataracts as the first neonatal sign of Fanconi-Bickel syndrome.
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pubmed:affiliation |
Centro 'Fondazione Mariani' per le malattie metaboliche dell'Infanzia, Paediatric Clinic, University of Milan-Bicocca, Via Pergolesi 33, 20052, Monza, Italy. francesca.furlan@pediatriamonza.it
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pubmed:publicationType |
Journal Article,
Case Reports
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