EP03.08: Early prenatal diagnosis of fused cavum septi pellucidi (CSP) and fornix associated with dysgenic corpus callosum (CC): case report

2015 ◽  
Vol 46 ◽  
pp. 193-193
Author(s):  
F. Moretti ◽  
A. Alhasani ◽  
J. Hurteau ◽  
E. Miller
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Corpus Callosum ◽  
Cavum Septi Pellucidi

Prenatal diagnosis of an epignathus associated with a 49, XXXXY karyotype – a case report

2007 ◽  
Vol 28 (S 1) ◽  
Author(s):  
I Staboulidou ◽  
K Miller ◽  
G Göhring ◽  
P Hillemanns ◽  
M Wüstemann
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis

Mature teratoma splitting the brainstem in a newborn: case report

2019 ◽  
Vol 24 (4) ◽  
pp. 371-375
Author(s):  
Li-tal Pratt ◽  
Shelly I. Shiran ◽  
Ronit Precel ◽  
Liat Ben-Sira ◽  
Gustavo Malinger ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Posterior Fossa ◽  
Mature Teratoma

Mature teratomas (MTs) of the posterior fossa are extremely rare. The authors present a case of a prenatal diagnosis of an MT splitting the brainstem. Representative images as well as the clinical and surgical course are presented. Literature regarding “split brainstem” and MT of the posterior fossa is discussed.

A case of prenatal diagnosis of corpus callosum lipoma

2020 ◽  
Author(s):  
A.I. Zamiatina, M.V. Medvedev
Keyword(s):  
Magnetic Resonance Imaging ◽  
Blood Flow ◽  
Prenatal Diagnosis ◽  
Magnetic Resonance ◽  
Corpus Callosum ◽  
Color Doppler ◽  
Septum Pellucidum ◽  
Resonance Imaging

A case of prenatal diagnosis of the corpus callosum lipoma at 32–33 weeks of gestation is presented. In a consultative examination, a hyperechoic formation with clear contours was found in the projection of the septum pellucidum, occupying the rostrum, genu, and truncus of corpus callosum, without signs of intratumorally blood flow in the color Doppler mapping mode. The prenatal diagnosis of "callosum lipoma" was established, confirmed after the birth of a child during magnetic resonance imaging.

scholarly journals Molecular characterization of an analphoid supernumerary marker chromosome derived from 18q22.1→qter in prenatal diagnosis: a case report

2014 ◽  
Vol 7 (1) ◽  
Author(s):  
Vincenzo Altieri ◽  
Oronzo Capozzi ◽  
Maria Cristina Marzano ◽  
Oriana Catapano ◽  
Immacolata Di Biase ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Molecular Characterization ◽  
Marker Chromosome

P09.07: Prenatal diagnosis of Klippel Trenaunay syndrome: a case report

2010 ◽  
Vol 36 (S1) ◽  
pp. 202-202
Author(s):  
M. Brain Giannotti ◽  
O. Gomez ◽  
N. Masoller ◽  
J. Martinez ◽  
B. Puerto ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Klippel Trenaunay Syndrome
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