scholarly journals P03.09: Prenatal diagnosis of restrictive foramen ovale: a case report

2010 ◽  
Vol 36 (S1) ◽  
pp. 176-176
Author(s):  
R. S. Abu-Rustum ◽  
L. Daou ◽  
M. Zaghloul
2018 ◽  
Vol 47 (2) ◽  
pp. 104-106
Author(s):  
Takashi Murakami ◽  
Lisheng Lin ◽  
Takumi Ishiodori ◽  
Syusuke Takeuchi ◽  
Junko Shiono ◽  
...  

2018 ◽  
Vol 5 (3) ◽  
pp. 159-162 ◽  
Author(s):  
Shyama Devadasan ◽  
Meenu Batra ◽  
Bijoy Balakrishnan ◽  
P. S. Sreeja ◽  
N. Patil Swapneel ◽  
...  

2011 ◽  
Vol 139 (3-4) ◽  
pp. 221-224
Author(s):  
Vladimir Kuburovic ◽  
Vladislav Vukomanovic ◽  
Jovan Kosutic ◽  
Sanja Rakic ◽  
Slobodan Gazikalovic ◽  
...  

Introduction. Adams-Oliver syndrome is characterized by congenital aplasia of the vertex skin of the skull in combination with skull and transverse limb defects. Case Outline. We presented a 5-month old female infant with Adams-Oliver syndrome manifested as cutis marmorata, dilated scalp veins and limb reduction defects. Clinical manifestation also included thumb hypoplasia and extreme hypoplasia of other fingers, with agenesis of all toes on both feet. Echocardiogram revealed foramen ovale apertum. Venography showed dilated malformed scalp and neck veins, predominantly on the right side. On the basis of the clinical features and extended investigation we confirmed Adams-Oliver syndrome in the presented patient. Conclusion. We recommended prenatal diagnosis in case of future pregnancies, ultrasound examination, and follow-up of foetal anomalies.


2007 ◽  
Vol 50 (3) ◽  
pp. 268
Author(s):  
Ji Joung Lee ◽  
Min A Lee ◽  
Yun ee Rhee ◽  
Mea Young Chang ◽  
Hong Ryang Kil

2014 ◽  
Vol 5 (10) ◽  
pp. 529-531
Author(s):  
Renata Bokiniec ◽  
Katarzyna Kufel ◽  
Maria K. Borszewska-Kornacka ◽  
Joanna Szymkiewicz-Dangel

Author(s):  
I Staboulidou ◽  
K Miller ◽  
G Göhring ◽  
P Hillemanns ◽  
M Wüstemann

2019 ◽  
Vol 24 (4) ◽  
pp. 371-375
Author(s):  
Li-tal Pratt ◽  
Shelly I. Shiran ◽  
Ronit Precel ◽  
Liat Ben-Sira ◽  
Gustavo Malinger ◽  
...  

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.


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