2015
DOI: 10.1016/j.crad.2014.11.004
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Antenatal diagnosis of agenesis of the corpus callosum

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Cited by 43 publications
(39 citation statements)
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“…Ultrasound guidelines suggest reserving MRI examination to those fetuses where there is a suspicion of abnormality on ultrasound . The ability of MRI to detect abnormalities not seen on ultrasound in this group of patients is as yet unknown, although evidence from other cohorts suggests that significant abnormalities may be detected …”
Section: Fetal Neurological Assessment and Antenatal Diagnosismentioning
confidence: 91%
See 1 more Smart Citation
“…Ultrasound guidelines suggest reserving MRI examination to those fetuses where there is a suspicion of abnormality on ultrasound . The ability of MRI to detect abnormalities not seen on ultrasound in this group of patients is as yet unknown, although evidence from other cohorts suggests that significant abnormalities may be detected …”
Section: Fetal Neurological Assessment and Antenatal Diagnosismentioning
confidence: 91%
“…67 The ability of MRI to detect abnormalities not seen on ultrasound in this group of patients is as yet unknown, although evidence from other cohorts suggests that significant abnormalities may be detected. 66 The majority of fetal MRI is still being carried out at 1.5 T, but several units are using 3 T for research and clinical practice. Fetal MRI is usually acquired without resorting to maternal sedation, but as for any MRI examination maternal contraindications include: claustrophobia, metallic implants, some cardiac pacemakers, being overweight or obese (new wide-bore magnets with a diameter of 70 cm [rather than 60 cm] may be better tolerated by those with a high BMI or with claustrophobia).…”
Section: Fetal Brain Mri Assessment In Chdsmentioning
confidence: 99%
“…For example, the absence of the cavum septum pellucidum (CSP) and teardrop‐configured lateral ventricles, with possible ventriculomegaly (VM), raise suspicions that there is agenesis of the corpus callosum (ACC). A more definitive diagnosis is usually made through the nonvisualization of the corpus callosum (CC) in either sagittal or coronal plane …”
Section: Introductionmentioning
confidence: 99%
“…The findings in this case suggest that CT angiography or MRI may detect persistent POA more effectively in cases involving ACC. is complete in its craniocaudal extent by 18 to 19 weeks, although further maturation and growth continues into postnatal life [1]. Early disruption in the maturation of the corpus callosum can lead to a developmental condition known as ACC, a relatively frequent congenital malformation ranging from complete absence to hypo genesis of corpus callosum fibers.…”
Section: Introductionmentioning
confidence: 99%
“…ACC results from commissural defects, and although it can occur for a number of reasons, including genetic, metabolic, or vascular abnormalities, in most cases, the cause remains unknown [1]. Brain anomalies and other malformations associated with ACC include lipoma of the corpus callosum, cerebellar hypoplasia, Dandy-Walker syndrome, hydrocephalus due to obstruction of the foramen of Monro or aqueduct stenosis, interhemispheric cyst, porencephalic cyst, and neuronal migration disorders [2].…”
Section: Introductionmentioning
confidence: 99%