作者: Yaqiong Chai , Julie Coloigner , Adam M Bush , John C Wood , Natasha Lepore
DOI:
关键词:
摘要: Sickle Cell Disease (SCD) is a genetic anemia with a high vascular occlusion occurrence rate. Detecting regional cerebral blood flow (CBF) abnormalities plays an important role in identifying SCD patients at risk of developing silent infarcts. Regional and global CBF for 7 adolescent SCD were measured using pseudo-continuous arterial spin labeling MRI, compared with the ones in 7 controls. Average CBF values were higher in patients (p= 0.01) in all cerebral artery territories.