CareLit · DOI-Nachweis · Klinische Neurophysiologie
Rapidly-progressive Moyamoya syndrome associated with Bartonella henselae infection and Factor V Leiden mutation
DOI 10.1055/s-2006-939161
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Nachweis in CareLit
Autor:innenA Hahn, R Siekmann, B Neubauer
ZeitschriftKlinische Neurophysiologie
Ausgabe03/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Introduction: Moyamoya syndrome (MMS) is characterized by progressive stenosis of the distal internal carotid artery (ICA) and proximal cerebral arteries accompanied by an extensive collateral vascular network at the base of the brain. Case: We report on a now 24-month-old Caucasian girl who developed right-sided hemiparesis at age 19 months. An MRI revealed an infarction in the territory of the left median cerebral…
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Zitierempfehlung
A Hahn, R Siekmann, B Neubauer (2006) Rapidly-progressive Moyamoya syndrome associated with Bartonella henselae infection and Factor V Leiden mutation. Klinische Neurophysiologie (03). https://doi.org/10.1055/s-2006-939161
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