Prenatal diagnosis of fetal heterotaxy syndrome by ultrasound: A case report

2019 ◽  
Vol 148 (2) ◽  
pp. 262-263
Author(s):  
Yuan Wang ◽  
Xu Zhao ◽  
Tingting Ge
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Heterotaxy Syndrome

scholarly journals EP16.09: Prenatal diagnosis of fetal heterotaxy syndrome by ultrasound: a case report

2019 ◽  
Vol 54 (S1) ◽  
pp. 327-327
Author(s):  
X. Zhao ◽  
Y. Wang ◽  
T. Ge ◽  
W. Chen
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Heterotaxy Syndrome

scholarly journals P03.11: Prenatal diagnosis of heterotaxy syndrome at 13 + 5 weeks of gestation: a case report

2010 ◽  
Vol 36 (S1) ◽  
pp. 177-177
Author(s):  
A. Gerede ◽  
F. Rouvalis ◽  
A. Athanasiadis ◽  
E. A. Assimakopoulos ◽  
B. C. Tarlatzis
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Heterotaxy Syndrome

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.

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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