Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutation

被引:45
作者
Greenberg, SM
Shin, Y
Grabowski, TJ
Cooper, GE
Rebeck, GW
Iglesias, S
Chapon, F
Tournier-Lasserve, E
Baron, JC
机构
[1] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Univ Iowa, Coll Med, Dept Neurol & Radiol, Iowa City, IA USA
[4] Sanders Brown Ctr Aging, Lexington, KY USA
[5] Univ Caen, INSERM, U320, F-14032 Caen, France
[6] Fac Med Lariboisiere, INSERM, EMI 9921, Paris, France
[7] Hop AP HP Lariboisiere, Paris, France
[8] Univ Cambridge, Dept Neurol, Cambridge CB2 1TN, England
关键词
D O I
10.1212/01.WNL.0000050140.10044.A8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The authors searched for mutations in the beta-amyloid precursor protein in a Spanish family with a hereditary syndrome of hemorrhagic stroke, dementia, leukoencephalopathy, and occipital calcifications. DNA from two affected members demonstrated the Iowa amyloid precursor protein mutation previously identified as a cause of severe amyloid angiopathy without hemorrhagic stroke. These data point to other genetic or environmental factors that may determine the occurrence of symptomatic hemorrhage in amyloid angiopathy.
引用
收藏
页码:1020 / 1022
页数:3
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