Research Studies Archive

Agenesis of the corpus callosum in California 1983-2003: a population-based study

Abstract The objective of this study was to characterize the prevalence, demographic risk factors, and ...

Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations

Abstract Objective: We sought to categorize the structural brain anomalies associated with abnormalities of ...

Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies

Abstract Absence of the corpus callosum is often associated with cognitive deficits, autism, and epilepsy. ...

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

Abstract Brain malformations involving the corpus callosum are common in children with developmental ...

Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia

Abstract The corpus callosum is the principal cerebral commissure connecting the right and left hemispheres. ...

Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families

Abstract Objective: We sought to create a classification system for pediatric corpus callosal abnormalities ...

Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders

Abstract Objective: BCORL1, a transcriptional co-repressor, has a role in cortical migration, neuronal ...

Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities

Abstract The collapsin response mediator protein (CRMP) family proteins are intracellular mediators of ...

De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities

Abstract Introduction: Whole-exome sequencing (WES) has identified de novo variants in chromatin remodelling ...

Outcome of Rare Fetal Septal and Callosal Anomalies: A Systematic Review and Meta-Analysis

Abstract Objectives: To report the outcome of isolated rare anomalies of the cavum septi pellucidum (CSP) and ...

Demographic, ocular and associated neurological findings in corpus callosum malformations

Abstract Background: The corpus callosum is a primary commissural part of the brain which connects the two ...

Prenatal genetic testing in 19 fetuses with corpus callosum abnormality

Abstract Background: Corpus callosum abnormality (CCA) can lead to epilepsy, moderate severe neurologic or ...
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