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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1989-6-12
|
| pubmed:abstractText |
Oculomotor apraxia may be idiopathic or a symptom of a variety of diseases. In Gaucher disease, oculomotor deficit is characterized by a failure of volitional horizontal gaze with preservation of vertical movements. We present 2 sisters, 6 1/2 and 5 1/2 years of age, in whom the presenting sign was oculomotor apraxia. Oculomotor apraxia has not been previously reported as the presenting manifestation of Gaucher disease.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0887-8994
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
5
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
128-9
|
| pubmed:dateRevised |
2006-5-23
|
| pubmed:meshHeading | |
| pubmed:articleTitle |
Oculomotor apraxia: the presenting sign of Gaucher disease.
|
| pubmed:affiliation |
Neuropediatric Unit, Bikur Cholim Hospital, Jerusalem, Israel.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|