| Literature DB >> 27381655 |
Yu Kobayashi1, Shinichi Magara2, Kenichi Okazaki2, Takao Komatsubara2, Hirotomo Saitsu3, Naomichi Matsumoto3, Mitsuhiro Kato4, Jun Tohyama5.
Abstract
Megalencephalic polymicrogyria syndromes include megalencephaly-capillary malformation and megalencephaly-polymicrogyria-polydactyly-hydrocephalus. Recent genetic studies have identified that genes in the PI3K-AKT pathway are involved in the pathogenesis of these disorders. Herein, we report a patient who presented with developmental delay, epilepsy and peculiar neuroimaging findings of megalencephaly, polymicrogyria, and symmetrical band heterotopia in the periventricular region. The heterotopias exhibited inhomogeneous signals with undulatory mixtures of gray and white matter, resembling ribbon-like heterotopia, with a predominance in the temporal to occipital regions. These neuroradiological findings were not consistent with those in known megalencephalic polymicrogyria syndromes. No genetic abnormality was identified through whole-exome sequencing. The neuroimaging findings of this patient may represent a novel cortical malformation involving megalencephaly with polymicrogyria and ribbon-like band heterotopia.Entities:
Keywords: Cortical malformation; Megalencephaly; Polymicrogyria; Ribbon-like heterotopia; Subcortical heterotopia
Mesh:
Year: 2016 PMID: 27381655 DOI: 10.1016/j.braindev.2016.06.004
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961