scholarly journals Mapping Fetal Brain Development In Utero Using Magnetic Resonance Imaging: The Big Bang of Brain Mapping

2011 ◽  
Vol 13 (1) ◽  
pp. 345-368 ◽  
Author(s):  
Colin Studholme
2017 ◽  
Vol 43 (2) ◽  
pp. 113-122 ◽  
Author(s):  
Daphna Link ◽  
Michael B. Braginsky ◽  
Leo Joskowicz ◽  
Liat Ben Sira ◽  
Shaul Harel ◽  
...  

2006 ◽  
Vol 30 (4) ◽  
pp. 299 ◽  
Author(s):  
D. Prayer ◽  
G. Kasprian ◽  
E. Krampl ◽  
B. Ulm ◽  
L. Witzani ◽  
...  

US Neurology ◽  
2010 ◽  
Vol 05 (02) ◽  
pp. 89
Author(s):  
Hao Huang ◽  

Human brain anatomy is characterized by dramatic structural changes during fetal development. It is extraordinarily complex and yet its origin is asimple tubular structure. Revealing detailed anatomy at different stages of human fetal brain development not only aids in understanding this highlyordered process, but also provides clues to detect abnormalities caused by genetic or environmental factors. For example, the characterization ofwhite matter axon growth could provide important clues to understanding the inhomegeneity of white matter injuries in cerebral palsy. However,anatomical studies of human brain development during this period are surprisingly scarce, and histology-based atlases have only recently becomeavailable. Diffusion tensor imaging (DTI), a novel method of magnetic resonance imaging (MRI), is capable of delineating anatomical components withhigh contrast and revealing structures at the microscopic level. The volumetric measurement from 3D DTI data can quantify structural growth. Asdiscussed in this article, the fetal brain DTI database will be a valuable resource for human brain developmental study and will provide referencestandards for diagnostic radiology of premature newborns.


2017 ◽  
Vol 72 (5) ◽  
pp. 427.e1-427.e8 ◽  
Author(s):  
M. Paddock ◽  
R. Akram ◽  
D.A. Jarvis ◽  
P. Armitage ◽  
S. Song ◽  
...  

Author(s):  
Rachel L. Leon ◽  
Imran N. Mir ◽  
Christina L. Herrera ◽  
Kavita Sharma ◽  
Catherine Y. Spong ◽  
...  

Abstract Children with congenital heart disease (CHD) are living longer due to effective medical and surgical management. However, the majority have neurodevelopmental delays or disorders. The role of the placenta in fetal brain development is unclear and is the focus of an emerging field known as neuroplacentology. In this review, we summarize neurodevelopmental outcomes in CHD and their brain imaging correlates both in utero and postnatally. We review differences in the structure and function of the placenta in pregnancies complicated by fetal CHD and introduce the concept of a placental inefficiency phenotype that occurs in severe forms of fetal CHD, characterized by a myriad of pathologies. We propose that in CHD placental dysfunction contributes to decreased fetal cerebral oxygen delivery resulting in poor brain growth, brain abnormalities, and impaired neurodevelopment. We conclude the review with key areas for future research in neuroplacentology in the fetal CHD population, including (1) differences in structure and function of the CHD placenta, (2) modifiable and nonmodifiable factors that impact the hemodynamic balance between placental and cerebral circulations, (3) interventions to improve placental function and protect brain development in utero, and (4) the role of genetic and epigenetic influences on the placenta–heart–brain connection. Impact Neuroplacentology seeks to understand placental connections to fetal brain development. In fetuses with CHD, brain growth abnormalities begin in utero. Placental microstructure as well as perfusion and function are abnormal in fetal CHD.


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