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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2006-2-28
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pubmed:abstractText |
We report on a 9-year-old girl who was referred to our department because of increasing macrocephaly and school problems. The neurological examination disclosed mild cerebellar dysfunction and positive pyramidal tract signs. An MRI of the brain revealed extensive signal alterations of the white matter. Biochemical investigations established the diagnosis of L-2-hydroxyglutaric aciduria which has to be kept in mind as a rare cause of macrocephaly.
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pubmed:language |
ger
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|
pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
0300-8630
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
218
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
72-3
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:16506106-Adolescent,
pubmed-meshheading:16506106-Age Factors,
pubmed-meshheading:16506106-Brain,
pubmed-meshheading:16506106-Brain Diseases, Metabolic, Inborn,
pubmed-meshheading:16506106-Child,
pubmed-meshheading:16506106-Child, Preschool,
pubmed-meshheading:16506106-Female,
pubmed-meshheading:16506106-Glutarates,
pubmed-meshheading:16506106-Humans,
pubmed-meshheading:16506106-Hydroxy Acids,
pubmed-meshheading:16506106-Infant,
pubmed-meshheading:16506106-Intellectual Disability,
pubmed-meshheading:16506106-Magnetic Resonance Imaging,
pubmed-meshheading:16506106-Neurologic Examination
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pubmed:articleTitle |
[L-2-hydroxyglutaric aciduria -- a rare cause of macrocephaly].
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pubmed:affiliation |
Abteilung für Neuropädiatrie und Sozialpädiatrie, Universitätsklinikum Giessen. Olaf.Hussmann@paediat.med.uni-giessen.de
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pubmed:publicationType |
Journal Article,
Comparative Study,
English Abstract,
Case Reports
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