𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Prenatal diagnosis of schizencephaly with 2D-3D sonography and MRI

✍ Scribed by Ali Gedikbasi; Gokhan Yildirim; Sezin Saygi; Oguz Arslan; Ahmet Gul; Yavuz Ceylan

Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
188 KB
Volume
37
Category
Article
ISSN
0091-2751

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

We report a case of schizencephaly diagnosed prenatally at 23 weeks of gestational age with two‐dimensional (2D) and three‐dimensional (3D) sonography and fetal brain MRI, confirmed by autopsy. The diagnostic method of choice is 2D transabdominal and transvaginal sonography, whereas additional 3D sonography and MRI may provide a better understanding of the pathology and related findings. © 2009 Wiley Periodicals, Inc. J Clin Ultrasound, 2009

📜 SIMILAR VOLUMES

Prenatal diagnosis of unilateral megalen
Prenatal diagnosis of unilateral megalencephaly by 2D and 3D ultrasound: a case report
✍ E. Hafner; W. Bock; G. Zoder; K. Schuchter; A. Rosen; M. Plattner 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 191 KB 👁 2 views

Unilateral megalencephaly is a rare malformation of the central nervous system characterized by an overgrowth of one cerebral hemisphere due to an anomaly of neuronal cell migration. It shows macroscopic and histological alterations of the central nervous tissue. We report on a case of this malform

Prenatal diagnosis by 3D ultrasound and
Prenatal diagnosis by 3D ultrasound and MRI of an unusual malformation of cortical development with brain-in-brain appearance
✍ Luca Valsecchi; Paolo Cavoretto; Lara Di Piazza; Maddalena Smid; Silvia Pontesil 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 266 KB 👁 1 views

## Abstract A 31‐year‐old pregnant woman was referred for isolated mild ventriculomegaly and failure to visualize the left lateral ventricle's anterior horn on second trimester sonography (US). Three‐dimensional US suspected a frontal lesion deviating the midline. MRI revealed a mass compressing th

Prenatal diagnosis of holoprosencephaly
Prenatal diagnosis of holoprosencephaly with ethmocephaly via 3-dimensional sonography
✍ Gui-Se-Ra Lee; Soo Young Hur; Jong-Chul Shin; Soo-Pyung Kim; Sa Jin Kim 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 199 KB

We present the prenatal 3-dimensional (3D) sonographic findings in a case of holoprosencephaly with ethmocephaly at 32 weeks' gestation. The sonographic diagnosis was based on the intracranial findings of a single ventricle and bulb-shaped appearance of the thalami and facial abnormalities, includin

Intra- and interobserver variability of
Intra- and interobserver variability of 2D and 3D transvaginal sonography in the diagnosis of benign versus malignant adnexal masses
✍ Maria A. Pascual; Betlem Graupera; Lourdes Hereter; Anna Rotili; Ignacio Rodrigu 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 357 KB

## Abstract ## Purpose. The purpose of this study was to investigate the intraobserver and interobserver agreements in the diagnosis of malignant versus benign adnexal masses using two‐dimensional ultrasonography (2D US) and three‐dimensional ultrasonography (3D US). ## Methods. Two experienced

Spatially encoded phase-contrast MRI—3D
Spatially encoded phase-contrast MRI—3D MRI movies of 1D and 2D structures at millisecond resolution
✍ Klaus-Dietmar Merboldt; Martin Uecker; Dirk Voit; Jens Frahm 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 497 KB

## Abstract This work demonstrates that the principles underlying phase‐contrast MRI may be used to encode spatial rather than flow information along a perpendicular dimension, if this dimension contains an MRI‐visible object at only one spatial location. In particular, the situation applies to 3D

D-2-hydroxyglutaric aciduria: A case wit
D-2-hydroxyglutaric aciduria: A case with an intermediate phenotype and prenatal diagnosis of two affected fetuses
✍ Clarke, Nigel F. ;Andrews, Ian ;Carpenter, Kevin ;Jakobs, Cornelis ;van der Knaa 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 137 KB 👁 2 views

D-2-hydroxyglutaric aciduria (D2HGA) is a rare autosomal recessive disorder with variable clinical expression. The biochemical defect is unknown at present. Previously reported cases have either followed a severe clinical course characterized by neonatal epileptic encephalopathy, cortical blindness,