| Literature DB >> 17343267 |
Aslan Guzel1, Mehmet Tatli, Kaya Bilguvar, Michael L Diluna, Betul Bakkaloglu, Ali K Ozturk, Fatih Bayrakli, Murat Gunel.
Abstract
We report on an apparently new syndrome in a consanguineous family with seven members, three of whom have cerebral anomalies including pachygyria and arachnoid cysts along with mental retardation and seizures. The two patients with seizure disorders also had multiple enlarged perivascular spaces seen in the white matter of the centrum semiovale. Our data provide a contribution to the accumulating knowledge on familial cerebral anomalies including arachnoid cysts and lissencephaly. Given the lack of mutation in known lissencephaly genes such as LIS1, 14-3-3epsilon, and DCX, this syndrome may constitute a new phenotype with autosomal recessive inheritance.Entities:
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Year: 2007 PMID: 17343267 DOI: 10.1002/ajmg.a.31640
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802