Source:http://linkedlifedata.com/resource/pubmed/id/20117750
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2010-2-1
|
pubmed:abstractText |
We describe two children from a consanguineous family who manifested mega-corpus callosum, polymicrogyria, and psychomotor retardation. These patients also exhibited the brain anomalies of pontine hypoplasia and an abnormal cerebellar vermis. Our report confirms the genetic nature of megalencephaly-polymicrogyria-mega-corpus callosum syndrome, suggests a possible autosomal-recessive inheritance, and expands the spectrum of this rare entity.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
1873-5150
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
42
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
129-32
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:20117750-Agenesis of Corpus Callosum,
pubmed-meshheading:20117750-Child,
pubmed-meshheading:20117750-Child, Preschool,
pubmed-meshheading:20117750-Female,
pubmed-meshheading:20117750-Humans,
pubmed-meshheading:20117750-Male,
pubmed-meshheading:20117750-Malformations of Cortical Development,
pubmed-meshheading:20117750-Pedigree,
pubmed-meshheading:20117750-Psychomotor Disorders,
pubmed-meshheading:20117750-Syndrome
|
pubmed:year |
2010
|
pubmed:articleTitle |
Mega-corpus callosum, polymicrogyria, and psychomotor retardation syndrome.
|
pubmed:affiliation |
Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, India.
|
pubmed:publicationType |
Journal Article,
Case Reports
|