Linked Life Data

2494854

Source:http://linkedlifedata.com/resource/pubmed/id/2494854

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1989-4-24
pubmed:abstractText
Callosal dysgenesis implies a malformation of the corpus callosum with origins in the embryogenesis of the telencephalon. A retrospective review of 15 cases of callosal dysgenesis revealed three distinct categories: agenesis (three subjects), hypogenesis (nine subjects), and hypoplasia (three subjects). The basis of this distinction rests upon considerations of neural tube closure, formation and maintenance of the inductive plate of the massa commissuralis, and migration of the neuronal elements of the cerebral cortex responsible for the projection of the commissural fibers of the corpus callosum. These processes are somewhat interdependent in their expression and consequence, resulting in a unique mosaic of callosal and cortical gray matter and hemispheric white matter configurations that have individually varying clinicoradiologic manifestations.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:issn
0195-6108
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
339-44
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed:articleTitle
MR imaging of callosal and corticocallosal dysgenesis.
pubmed:affiliation
Huntington Medical Research Institutes, MR Imaging, Pasadena, CA 91105.
pubmed:publicationType
Journal Article