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  • 1
    Electronic Resource
    Electronic Resource
    Cerebral venous drainage via the ophthalmic veins in the Sturge-Weber syndrome (1994)
    Springer
    Neuroradiology 36 (1994), S. 318-320 
    Details
    ISSN: 1432-1920
    Keywords: Sturge-Weber syndrome ; Angiography ; Venous anomalies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We describe a 23-year-old girl with an extremely uncommon form of cerebral venous drainage and cerebellar leptomeningeal angiomatosis as a possible variant of the Sturge-Weber syndrome. Extensive congenital portwine stains all over the body, hypoplastic left renal and subclavian and iliac veins, cardiomegaly and ptosis and hypoplasia of the left kidney had been recognised in early childhood. She rapidly developed signs of intracranial hypertension. CT and MRI showed a right medial temporal lesion. Angiography revealed cerebellar pial angiomatosis with enlarged medullary veins and no functioning sigmoid sinuses or jugular veins. Cerebral venous drainage was via enlarged ophthalmic veins. Although the intracranial venous abnormalities were characteristic of the Sturge-Weber syndrome anomalies beyond the encephalofacial territory suggested a more complex developmental abnormality.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00593271
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Moyamoya with arterial anomalies: relevance to pathogenesis (1997)
    Springer
    Neuroradiology 39 (1997), S. 852-856 
    Details
    ISSN: 1432-1920
    Keywords: Key words Moyamoya disease ; Cerebrovascular anomalies ; Pathogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We report five patients with moyamoya associated with arterial anomalies, including five aneurysms, one with ectasia of the parent artery, a basilar artery fenestration and an arteriovenous malformation. Possible pathogenetic factors for moyamoya are discussed, and a prenatal origin is suggested.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s002340050519
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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