scholarly journals Fetal iGRASP cine CMR assisting in prenatal diagnosis of complicated cardiac malformation with impact on delivery planning

2019 ◽  
Vol 39 (4) ◽  
pp. 231-235 ◽  
Author(s):  
Misha Bhat ◽  
Kostas Haris ◽  
Sebastian Bidhult ◽  
Petru Liuba ◽  
Anthony H. Aletras ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Cardiac Malformation ◽  
Delivery Planning ◽  
Cine Cmr

scholarly journals Prenatal Diagnosis of Vein of Galen Aneurysmal Malformation Allows Early Transumbilical Endovascular Treatment

2020 ◽  
Vol 39 (03) ◽  
pp. 213-216 ◽  
Author(s):  
Zeferino Demartini ◽  
Gelson Luis Koppe ◽  
Luana A.M. Gatto ◽  
Ana Lucia Sarquis ◽  
Alexandre N. Francisco ◽  
...  
Keyword(s):  
Pulmonary Hypertension ◽  
Prenatal Diagnosis ◽  
Endovascular Treatment ◽  
Endovascular Therapy ◽  
Cardiac Failure ◽  
Early Treatment ◽  
Vein Of Galen ◽  
Umbilical Vessels ◽  
Delivery Planning ◽  
Perinatal Management

AbstractNeonates with vein of Galen aneurysmal malformation (VGAM) presenting with severe cardiac failure and pulmonary hypertension represent a challenge for endovascular therapy. When early treatment is required, the small femoral arteries in this population are usually difficult to cannulate. Alternatively, the umbilical vessels offer a natural pathway to reach the lesion. Therefore, prenatal diagnosis of VGAM allows for delivery planning, perinatal management, and embolization through umbilical approach, thus leading to better outcomes.

scholarly journals Complete atrioventricular septal defect in the era of prenatal diagnosis

2016 ◽  
Vol 18 (4) ◽  
pp. 500 ◽  
Author(s):  
Daniel Mureşan ◽  
Claudiu Mărginean ◽  
Gabriela Zaharie ◽  
Florin Stamatian
Keyword(s):  
Prenatal Diagnosis ◽  
Septal Defect ◽  
Transvaginal Ultrasound ◽  
First Trimester ◽  
Atrioventricular Septal Defect ◽  
Cardiac Malformation ◽  
Cardiac Malformations ◽  
Complete Atrioventricular Septal Defect ◽  
Complete Atrioventricular

Complete atrioventricular septal defect (CAVSD) is a fetal cardiac malformation (5% of all cardiac malformations) that can be detected prenatally with a reserved prognosis. The diagnosis can be suspected early at the end of the first trimester using the transabdominal or transvaginal ultrasound approach. Generally, the diagnostic can be established during the mid-trimester scan at 19-24 weeks of gestation. The percentage of antenatal diagnostic of CAVSD is between 57-92%. This review aims to analyze the anatomical principles and the ultrasound techniques that can improve the prenatal diagnosis of CAVSD. We have also analyzed the structural and genetic anomalies frequently associated with CAVSD.

scholarly journals Prenatal diagnosis of a complex fetal cardiac malformation associated with asplenia.

Heart ◽  
1991 ◽  
Vol 65 (5) ◽  
pp. 293-295 ◽  
Author(s):  
I Mauser ◽  
J Deutinger ◽  
G Bernaschek
Keyword(s):  
Prenatal Diagnosis ◽  
Cardiac Malformation

scholarly journals Topsy-Turvy Heart with Aortopulmonary Window and Severe Airway Malacia: Prenatal Diagnosis and Review of the Literature

2021 ◽  
Author(s):  
Yahia Hejazi ◽  
Gurdeep Mann ◽  
Younes Boudjemline ◽  
Jai P. Udassi ◽  
Grace Van Leeuwen ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Unusual Case ◽  
Clinical Presentation ◽  
Aortopulmonary Window ◽  
Review Of The Literature ◽  
Cardiac Malformation ◽  
Clockwise Rotation ◽  
Rare Malformation ◽  
Brachiocephalic Arteries ◽  
Insight Into

AbstractThe topsy-turvy heart is a very rare cardiac malformation that involves a global 90° clockwise rotation of the heart along its long axis. This rotation results in the displacement of the great arteries and severe elongation and stretching of the brachiocephalic arteries and the bronchi. We present an unusual case of topsy-turvy heart diagnosed prenatally with a large aorto-pulmonary window and. This case gives an insight into the morphological details and clinical presentation of this rare malformation and its associated complications. We also present a review of the literature of this rare anomaly showing only 15 live cases that have been published with only three cases diagnosed prenatally.

Foetal echocardiography of transposition of the great arteries and common arterial trunk

2012 ◽  
Vol 22 (6) ◽  
pp. 671-676 ◽  
Author(s):  
Grace Freire ◽  
Michelle Miller ◽  
James Huhta
Keyword(s):  
Differential Diagnosis ◽  
Prenatal Diagnosis ◽  
Early Detection ◽  
Family Counselling ◽  
Common Arterial Trunk ◽  
Arterial Trunk ◽  
Delivery Planning ◽  
Conotruncal Anomalies

AbstractAdvances in foetal echocardiography allow detection of conotruncal anomalies such as transposition of the great arteries and common arterial trunk. Early detection of these anomalies is important for appropriate delivery planning, family counselling, and management. This manuscript will review the anatomic considerations, differential diagnosis, and foetal echocardiographic features of each of these malformations and review the importance of prenatal diagnosis and family counselling.

scholarly journals Prenatal ultrasound diagnosis of fetal giant left ventricular aneurysm： A case report

2021 ◽  
Author(s):  
Wenjing Guo ◽  
Dengcai Zhang ◽  
Tingting Yao ◽  
Bin Ma ◽  
Tian-gang Li
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Rare Case ◽  
Left Ventricular ◽  
Left Ventricular Aneurysm ◽  
Ventricular Aneurysm ◽  
Prenatal Ultrasonography ◽  
Cardiac Malformation ◽  
Congenital Cardiac Malformation ◽  
Ultrasound Technology

Fetal ventricular aneurysm is a rare congenital cardiac malformation that can occur in various cardiac cavities and often exists in isolation without other malformations. Modern ultrasound technology can assist the prenatal diagnosis of ventricular aneurysm. Herein, we will present a rare case of a giant left ventricular aneurysm detected by prenatal ultrasonography.

Prenatal diagnosis of isolated total anomalous systemic venous connection to the left atrium

2017 ◽  
Vol 27 (7) ◽  
pp. 1394-1397 ◽  
Author(s):  
Béatrice Miltner ◽  
Alain Jean Poncelet ◽  
Catherine Barrea
Keyword(s):  
Prenatal Diagnosis ◽  
Right Ventricular ◽  
Left Atrium ◽  
Venous Return ◽  
Cardiac Malformation ◽  
Caval Vein ◽  
Inferior Caval Vein ◽  
Congenital Cardiac Malformation

AbstractWe report the prenatal diagnosis and the neonatal follow-up of a patient with isolated total abnormal systemic venous connection to the left atrium. Right-sided and left-sided superior caval veins and the inferior caval vein were all connected to the left atrium. Pulmonary venous return was normal. This was associated with some right ventricular underdevelopment. To our knowledge, this is the first fetal description of this very rare congenital cardiac malformation.

A new strategy for prenatal diagnosis in a sporadic haemophilia B family

Haemophilia ◽  
2001 ◽  
Vol 7 (4) ◽  
pp. 416-418 ◽  
Author(s):  
M. Acquila ◽  
F. Bottini ◽  
A. Valetto ◽  
D. Caprino ◽  
P. G. Mori ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Haemophilia B ◽  
New Strategy
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