Perinatal Stroke

2012 ◽  
Vol 224 (07) ◽  
Author(s):  
D Mu
Keyword(s):  
Author(s):  
Judy S. Reilly ◽  
Lara R. Polse

With respect to language, it has long been observed that children who experience early unilateral brain injury do not show the same irreparable damage as do adults with homologous late-onset strokes. Neural plasticity has been proposed as the explanation for such differential linguistic profiles; that is, the plasticity of the young, developing brain allows the possibility for extensive adaptation and organization following a neural insult. Recent research, however, suggests that there are limits to this ability to adapt and organize. Results from a another communicative system, affect, suggest that children with unilateral pre- or perinatal stroke show similar (albeit subtler) effects to adults with homologous late-onset injuries. This chapter presents findings on language development in children who sustained a pre- or perinatal unilateral stroke, and complements these studies with a discussion of affective expression in these same children. These prospective studies of children with perinatal stroke provide a unique window into the development of the neural substrates for language and affect. Specifically, they afford a context to investigate the degree to which particular brain regions may be privileged for specific behavioral functions, as well as how the developing brain adapts to organize alternative pathways in the wake of an early insult.


2019 ◽  
Vol 21 ◽  
pp. 101660 ◽  
Author(s):  
Brandon T. Craig ◽  
Helen L. Carlson ◽  
Adam Kirton
Keyword(s):  

2016 ◽  
Vol 2016 ◽  
pp. 1-11 ◽  
Author(s):  
Nigul Ilves ◽  
Pilvi Ilves ◽  
Rael Laugesaar ◽  
Julius Juurmaa ◽  
Mairi Männamaa ◽  
...  

Perinatal stroke is a leading cause of congenital hemiparesis and neurocognitive deficits in children. Dysfunctions in the large-scale resting-state functional networks may underlie cognitive and behavioral disability in these children. We studied resting-state functional connectivity in patients with perinatal stroke collected from the Estonian Pediatric Stroke Database. Neurodevelopment of children was assessed by the Pediatric Stroke Outcome Measurement and the Kaufman Assessment Battery. The study included 36 children (age range 7.6–17.9 years): 10 with periventricular venous infarction (PVI), 7 with arterial ischemic stroke (AIS), and 19 controls. There were no differences in severity of hemiparesis between the PVI and AIS groups. A significant increase in default mode network connectivity (FDR 0.1) and lower cognitive functions (p<0.05) were found in children with AIS compared to the controls and the PVI group. The children with PVI had no significant differences in the resting-state networks compared to the controls and their cognitive functions were normal. Our findings demonstrate impairment in cognitive functions and neural network profile in hemiparetic children with AIS compared to children with PVI and controls. Changes in the resting-state networks found in children with AIS could possibly serve as the underlying derangements of cognitive brain functions in these children.


2011 ◽  
Vol 171 (2) ◽  
pp. 225-234 ◽  
Author(s):  
Arvind Sehgal
Keyword(s):  

2009 ◽  
Vol 52 (2) ◽  
pp. 212-214 ◽  
Author(s):  
KAREN PYSDEN ◽  
PENNY FALLON ◽  
BHAGAVATHESWARAN MOORTHY ◽  
VIJEYA GANESAN

BMC Neurology ◽  
2005 ◽  
Vol 5 (1) ◽  
Author(s):  
Mohamed L Seghier ◽  
François Lazeyras ◽  
Slava Zimine ◽  
Sonja Saudan-Frei ◽  
Avinoam B Safran ◽  
...  

2011 ◽  
Vol 26 (S2) ◽  
pp. 1100-1100
Author(s):  
A. Matos-Pires ◽  
N. Cardoso-Pereira

Perinatal Stroke involves an often poorly understood neurocognitive events affecting the fetus and the new born with a potential for serious intellectual outcome.Our aim is to present a case study on the issue of neurocognitive defects on domains such as intellectual performance, attention and vigilance, executive functioning, visual perception, speed of processing, verbal learning and memory, and working memory on a 6 year old girl with perinatal arterial ischemic stroke.


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