scholarly journals Echogenic cavum septi pellucidi is associated with mild callosal dysgenesis on postnatal MRI

2019 ◽  
Vol 22 (3) ◽  
pp. 214-216
Author(s):  
Alexandra Stanislavsky ◽  
Stacy Goergen
2020 ◽  
Vol 11 (1) ◽  
pp. 21
Author(s):  
Claudia Brogna ◽  
Valentina Milano ◽  
Barbara Brogna ◽  
Lara Cristiano ◽  
Giuseppe Rovere ◽  
...  

The partial trisomy 13q encompasses an extensive variability of phenotypic and radiological findings including leukoencephalopathy and brain malformations such as holoprosencephaly, callosal dysgenesis, hippocampal hypoplasia, olfactory hypoplasia, and vermian hypoplasia. We report for the first time a case of a 23-year-old patient affected by de novo partial 13q22.1q34 trisomy (41.7 Mb, 72,365,975-114,077,122x3) presenting with hemiparesis related to both ischemic and haemorrhagic cerebral lesions compatible with cerebral vasculitis due to a possible combination of genetic and immunological interaction.


1998 ◽  
Vol 155 (8) ◽  
pp. 1074-1079 ◽  
Author(s):  
Peg C. Nopoulos ◽  
Jay N. Giedd ◽  
Nancy C. Andreasen ◽  
Judith L. Rapoport

1968 ◽  
Vol 10 ◽  
pp. 178b-179
Author(s):  
Tetsuya Leslie SASABE ◽  
Katsuhito AKAGI ◽  
Yoshikazu IWATA ◽  
Masatsugi KOBATAKE ◽  
Fujio UEMURA

1995 ◽  
Vol 44 (5) ◽  
pp. 471-475 ◽  
Author(s):  
Tadao Miyamori ◽  
Kahoko Miyamori ◽  
Takesi Hasegawa ◽  
Kazuhiko Tokuda ◽  
Yuuichi Yamamoto

2018 ◽  
Vol 210 (5) ◽  
pp. 989-997 ◽  
Author(s):  
Usha D. Nagaraj ◽  
Maria A. Calvo-Garcia ◽  
Beth M. Kline-Fath

2019 ◽  
Vol 54 (S1) ◽  
pp. 281-281
Author(s):  
J. Miguelez ◽  
M.H. Carvalho ◽  
E.Q. Barreto ◽  
W. Hisaba

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