2009
DOI: 10.1002/uog.7489
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Prenatal diagnosis and outcome of partial agenesis and hypoplasia of the corpus callosum

Abstract: Objective To present antenatal sonographic findings and outcome of fetuses with hypoplasia or partial agenesis of the corpus callosum. Methods

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Cited by 85 publications
(99 citation statements)
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References 24 publications
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“…intracranial masses, obstructive hydrocephalus (Davila-Gutuerrez, 2002;Paupe et al, 2002) rather than a primary malformative abnormality.Thus, callosal hypoplasia more likely depends upon an external factor affecting the number and size of callosal axons. This is apparently confirmed by a experience since callosal hypoplasia was often associated with additional brain anomalies (Ghi et al, 2010). Hypoplasia and partial agenesis of the corpus callosum may occur in isolation form, in these conditions, neurological outcome is reported by some to be similar to that in cases with absent corpus callosum1 ( Moutard et al ,2003;Mordefroid et al, 2004;Ghi et al, 2010).…”
Section: Callosal Hypoplasiamentioning
confidence: 66%
See 1 more Smart Citation
“…intracranial masses, obstructive hydrocephalus (Davila-Gutuerrez, 2002;Paupe et al, 2002) rather than a primary malformative abnormality.Thus, callosal hypoplasia more likely depends upon an external factor affecting the number and size of callosal axons. This is apparently confirmed by a experience since callosal hypoplasia was often associated with additional brain anomalies (Ghi et al, 2010). Hypoplasia and partial agenesis of the corpus callosum may occur in isolation form, in these conditions, neurological outcome is reported by some to be similar to that in cases with absent corpus callosum1 ( Moutard et al ,2003;Mordefroid et al, 2004;Ghi et al, 2010).…”
Section: Callosal Hypoplasiamentioning
confidence: 66%
“…This is apparently confirmed by a experience since callosal hypoplasia was often associated with additional brain anomalies (Ghi et al, 2010). Hypoplasia and partial agenesis of the corpus callosum may occur in isolation form, in these conditions, neurological outcome is reported by some to be similar to that in cases with absent corpus callosum1 ( Moutard et al ,2003;Mordefroid et al, 2004;Ghi et al, 2010). Callosal hypoplasia include a significant size reduction of the anterior genu, posterior genu (Walterfang, 2008, Walterfang, 2009aVidal et al, 2006;Just et al, 2007;Walterfang et al, 2009b;2009c), isthmus (Walterfang, 2008;Walterfang, 2009a;Vidal et al, 2006;Just et al, 2007;Cao et al, 2010)and the posterior midbody (Cao et al, 2010), a smaller splenium width (Bersani, 2010;Vidal et al, 2006;Just et al, 2007;Hutchinson et al ., 2008), a cyst in the splenium (Bamiou et al, 2007) and a smaller anterior midbody.…”
Section: Callosal Hypoplasiamentioning
confidence: 72%
“…24 Isolated complete agenesis, however, seems to have a better prognosis than a partial or hypoplastic corpus callosum. 19 A recent meta-analysis of 27 studies on the outcome shows a higher proportion of chromosomal anomalies, more gross and fine motor control affection, and a higher percentage of epilepsy in the partial agenesis group compared with the complete agenesis of the CC group. 40 Today, diagnosis relies on a midtrimester sonographic examination potentially revealing Յ1of the associated signs such as mild ventriculomegaly, colpocephaly, absent cavum septi pellucidi, upward displacement of the third ventricle, teardrop configuration of the lateral ventricles, or cystic dilation of the third ventricle.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, dysgenesis of the corpus callosum could be reflected by a misshapen or abnormal course of the pericallosal arteries and their branches. [18][19][20] With this study, we aimed to document the normal longitudinal development and variants of the pericallosal vasculature from 11 to 22 weeks of gestation using power Doppler flow and high-frequency sonography probes.…”
Section: Aimmentioning
confidence: 99%
“…Contudo, deve-se referir como principal limitação do plano médio sagital, a falta da clara diferenciação do CC em relação à porção inferior do septo pelúcido 6 . Além disso, os casos de hipoplasia e agenesia parcial do CC pela US2D são extremamente difíceis de serem realizados, porque apesar de o CC ser identificado com forma atípica, a forma da cabeça fetal no plano axial é frequentemente normal 7 .…”
Section: Introductionunclassified