scholarly journals IC-P-046: CEREBRAL AMYLOID ANGIOPATHY IS MORE SEVERE IN AUTOSOMAL DOMINANT AD CASES WITH CEREBRAL MICROHEMORRHAGES: RESULTS FROM THE DIAN STUDY

2019 ◽  
Vol 15 ◽  
pp. P48-P49
Author(s):  
Nelly Joseph-Mathurin ◽  
Richard J. Perrin ◽  
Nigel J. Cairns ◽  
Erin E. Franklin ◽  
Chengjie Xiong ◽  
...  
2019 ◽  
Vol 15 ◽  
pp. P1125-P1126
Author(s):  
Nelly Joseph-Mathurin ◽  
Richard J. Perrin ◽  
Nigel J. Cairns ◽  
Erin E. Franklin ◽  
Chengjie Xiong ◽  
...  

2021 ◽  
pp. 10.1212/CPJ.0000000000001055
Author(s):  
Mohamed Ridha ◽  
Yasmin Aziz ◽  
Joseph Broderick

A 67-year-old man was referred from ophthalmology for possible cerebral amyloid angiopathy (CAA) discovered during work-up of possible optic neuropathy. MRI (figure 1) demonstrated innumerable periventricular, brainstem, and cortical cerebral microhemorrhages (CMH). Scattered, non-specific white matter hyperintensities was seen on T2-weighted imaging without surrounding hypointense rim. He had no hypertension, and the distribution was uncharacteristic for CAA. Despite absent family history of stroke or seizure, testing for familial cerebral cavernous malformation (FCCM) identified a pathogenic mutation of KRIT1 (c.382G>T).


2005 ◽  
Vol 38 (1) ◽  
pp. 24-26 ◽  
Author(s):  
Anne Rovelet-Lecrux ◽  
Didier Hannequin ◽  
Gregory Raux ◽  
Nathalie Le Meur ◽  
Annie Laquerrière ◽  
...  

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