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Jang J.,Yonsei University | Quan Z.,Yonsei University | Quan Z.,Epilepsy Research Institute | Quan Z.,Yonsei Stem Cell Research Institute | And 12 more authors.
Biotechnology Journal | Year: 2014

The pathophysiological mechanisms underlying childhood neurological disorders have remained obscure due to a lack of suitable disease models reflecting human pathogenesis. Using induced pluripotent stem cell (iPSC) technology, various neurological disorders can now be extensively modeled. Specifically, iPSC technology has aided the study and treatment of early-onset pediatric neurodegenerative diseases such as Rett syndrome, Down syndrome, Angelman syndrome. Prader-Willi syndrome, Friedreich's ataxia, spinal muscular atrophy (SMA), fragile X syndrome, X-linked adrenoleukodystrophy (ALD), and SCN1A gene-related epilepsies. In this paper, we provide an overview of various gene delivery systems for generating iPSCs, the current state of modeling early-onset neurological disorders and the ultimate application of these in vitro models in cell therapy through the correction of disease-specific mutations. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Source

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