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rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
4
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|
pubmed:dateCreated |
1989-11-9
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|
pubmed:abstractText |
Urea cycle enzymopathies are rare in the literature. They are accompanied by neurological disorders somehow related to the increase in blood ammonia. Reviewing the possible physiopathological course we present a case in which during an eight month period severe cerebral atrophy developed, more intense in the occipital region but totally sparing the posterior cranial fossa structures.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
0028-3940
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|
pubmed:author |
|
|
pubmed:issnType |
Print
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|
pubmed:volume |
31
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
356-7
|
|
pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:2797431-Ammonia,
pubmed-meshheading:2797431-Atrophy,
pubmed-meshheading:2797431-Cerebral Cortex,
pubmed-meshheading:2797431-Female,
pubmed-meshheading:2797431-Humans,
pubmed-meshheading:2797431-Infant,
pubmed-meshheading:2797431-Intellectual Disability,
pubmed-meshheading:2797431-Ornithine Carbamoyltransferase Deficiency Disease,
pubmed-meshheading:2797431-Time Factors,
pubmed-meshheading:2797431-Tomography, X-Ray Computed
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|
pubmed:year |
1989
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|
pubmed:articleTitle |
Computerized tomography in primary hyperammonemia.
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|
pubmed:affiliation |
Department of Neuroradiology, Hospital de Navarra, Pamplona, Spain.
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|
pubmed:publicationType |
Journal Article,
Case Reports
|
