| Literature DB >> 20117750 |
Parayil S Bindu1, Arun B Taly, Sanjib Sinha, Rose D Bharath.
Abstract
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.Entities:
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Year: 2010 PMID: 20117750 DOI: 10.1016/j.pediatrneurol.2009.09.012
Source DB: PubMed Journal: Pediatr Neurol ISSN: 0887-8994 Impact factor: 3.372