scholarly journals Prenatal diagnosis of epignathus with multiple malformations in one fetus of a twin pregnancy using three-dimensional ultrasonography and magnetic resonance imaging

2015 ◽  
Vol 58 (1) ◽  
pp. 65 ◽  
Author(s):  
Na Rae Moon ◽  
Jae Young Min ◽  
Yeon Hee Kim ◽  
Sae Kyung Choi ◽  
Jong Chul Shin ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Prenatal Diagnosis ◽  
Magnetic Resonance ◽  
Twin Pregnancy ◽  
Three Dimensional ◽  
Resonance Imaging

Prenatal Diagnosis of Aneurysms of the Vein of Galen (Vena Magna Cerebri) With Conventional Sonography, Three-dimensional Sonography, and Magnetic Resonance Imaging

2003 ◽  
Vol 22 (12) ◽  
pp. 1363-1368 ◽  
Author(s):  
Franca A. Gerards ◽  
Melanie A. J. Engels ◽  
Frederik Barkhof ◽  
Frank A. M. van den Dungen ◽  
R. Jeroen Vermeulen ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Prenatal Diagnosis ◽  
Magnetic Resonance ◽  
Three Dimensional ◽  
Vein Of Galen ◽  
Resonance Imaging

Prenatal Diagnosis of a Large Axillary Cystic Lymphangioma by Three-dimensional Ultrasonography and Magnetic Resonance Imaging

2003 ◽  
Vol 22 (4) ◽  
pp. 419-423 ◽  
Author(s):  
Rodrigo Ruano ◽  
Jean-Pierre Aubry ◽  
Isabelle Simon ◽  
Anne-Gaelle Grebille ◽  
Pascale Sonigo ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Prenatal Diagnosis ◽  
Magnetic Resonance ◽  
Three Dimensional ◽  
Cystic Lymphangioma ◽  
Resonance Imaging

scholarly journals Craniosynostosis: prenatal diagnosis by 2D/3D ultrasound, magnetic resonance imaging and computed tomography.

2016 ◽  
Vol 18 (3) ◽  
pp. 378 ◽  
Author(s):  
Talita Micheletti Helfer ◽  
Alberto Borges Peixoto ◽  
Gabriele Tonni ◽  
Edward Araujo Júnior
Keyword(s):  
Magnetic Resonance Imaging ◽  
Computed Tomography ◽  
Prenatal Diagnosis ◽  
Magnetic Resonance ◽  
Three Dimensional ◽  
3D Ultrasound ◽  
Resonance Imaging ◽  
Perinatal Complications ◽  
Wide Range ◽  
Magnetic Resonance Imaging Mri

Craniosynostosis is defined as the process of premature fusion of one or more of the cranial sutures.  It is a common condition that occurs in about 1 to 2,000 live births. Craniosynostosis may be classified in primary or secondary. It is also classified as nonsyndromic or syndromic. According to suture commitment, craniosynostosis may affect a single suture or multiple sutures. There is a wide range of syndromes involving craniosynostosis and the most common are Apert, Pffeifer, Crouzon, Shaethre-Chotzen and Muenke syndromes. The underlying etiology of nonsyndromic craniosynostosis is unknown. Mutations in the fibroblast growth factor (FGF) signalling pathway play a crucial role in the etiology of craniosynostosis syndromes. Prenatal ultrasound`s detection rate of craniosynostosis is low. Nowadays, different methods can be applied for prenatal diagnosis of craniosynostosis, such as two-dimensional (2D) and three-dimensional (3D) ultrasound, magnetic resonance imaging (MRI), computed tomography (CT) scan and, finally, molecular diagnosis. The presence of craniosynostosis may affect the birthing process. Fetuses with craniosynostosis also have higher rates of perinatal complications. In order to avoid the risks of untreated craniosynostosis, children are usually treated surgically soon after postnatal diagnosis.

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