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[Moyamoya].
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- Author(s): Hansen RN;Hansen RN; Andersen G; Longin E
- Source:
Ugeskrift for laeger [Ugeskr Laeger] 2011 Jan 24; Vol. 173 (4), pp. 281-2.
- Publication Type:
Case Reports; Journal Article
- Language:
Danish
- Additional Information
- Transliterated Title:
Moyamoya.
- Source:
Publisher: Den Alm Danske Laegerforening Country of Publication: Denmark NLM ID: 0141730 Publication Model: Print Cited Medium: Internet ISSN: 1603-6824 (Electronic) Linking ISSN: 00415782 NLM ISO Abbreviation: Ugeskr Laeger Subsets: MEDLINE
- Publication Information:
Original Publication: Copenhagen : Den Alm Danske Laegerforening
- Subject Terms:
- Abstract:
The disease moyamoya is rare in Europe, but it is seen more frequently in Japan and other Asian countries. Moyamoya is characterized by progressing occlusion of the cerebral arteries and secondary development of pathological collateral vessels induced by ischaemia. This case report describes a newly diagnosed patient with moyamoya, who was referred to a paediatric clinic because of headache and involuntary movements and sounds. Due to the rare occurrence of moyamoya, the purpose of this case report is to draw attention to its diagnosis with a view to achieving an early diagnosis of the disease.
- Publication Date:
Date Created: 20110126 Date Completed: 20110222 Latest Revision: 20161125
- Publication Date:
20240829
- Accession Number:
21262175
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