Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1988-9-21
|
| pubmed:abstractText |
Case report of a 7 1/2-year-old girl considered as being normal until the age of 2 years. From then on she progressed with gait disturbance, mental deterioration, dystonic movements, convulsions and dysarthria. She died of bronchopneumonia one year later. CT scan showed hyperdensity at the putamen, with no signs of cerebral atrophy. Pathological examination disclosed an intense red coloration of the putamen and axonal "spheroids" at electron microscopy.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Mar
|
| pubmed:issn |
0004-282X
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
46
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
69-72
|
| pubmed:dateRevised |
2009-11-11
|
| pubmed:meshHeading |
pubmed-meshheading:3408385-Axons,
pubmed-meshheading:3408385-Basal Ganglia Diseases,
pubmed-meshheading:3408385-Child,
pubmed-meshheading:3408385-Female,
pubmed-meshheading:3408385-Humans,
pubmed-meshheading:3408385-Pantothenate Kinase-Associated Neurodegeneration,
pubmed-meshheading:3408385-Tomography, X-Ray Computed
|
| pubmed:year |
1988
|
| pubmed:articleTitle |
"Hallervorden-Spatz syndrome--infantile neuroaxonal dystrophy" complex. Case report.
|
| pubmed:affiliation |
Servico de Neurologia, Hospital do Servidor Público Estadual de São Paulo, Brasil.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|