Open Access

Schizencephaly Associated with Polymicrogirya – Cause for Late-Onset Epileptic Seizures in Adult. A Case Report.


Cite

1. Ropper, A., Samuels, M. & Klein, J. (2014). Adams and Victor’s Principles of Neurology 10th Edition: McGraw-Hill Education (pp 1005,1007,1016)Search in Google Scholar

2. Lipka, J., Kuijpers, M., Jaworski, J. & Hoogenraad, Casper C. (2013). Mutations in cytoplasmic dynein and its regulators cause malformations of cortical development and neurodegenerative diseases. Biochemical Society Transactions. 41(6), 1605-1612. doi: 10.1042/bst2013018810.1042/BST20130188Search in Google Scholar

3. Mirzaa, G.M., Conti, V., Timms, A.E., Smyser, C.D., Ahmed, S., Carter, M., Barnett, S., Hufnagel, R.B., Goldstein, A., Narumi-Kishimoto, Y., Olds, C., Collins, S., Johnston, K., Deleuze, J.F., Nitschke, P., Friend, K., Harris, C., Goetsch, A., Martin, B., Boyle, E.A., Parrini, E., Mei, D., Tattini, L., Slavotinek, A., Blair, E., Barnett, C., Shendure, J., Chelly, J., Dobyns, W.B. & Guerrini, R. (2015). Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study. Lancet Neurol. 14(12), 1182-1195. doi: 10.1016/s1474-4422(15)00278-1.10.1016/S1474-4422(15)00278-1Search in Google Scholar

4. Moon, H.M. & Wynshaw-Boris, A. (2013). Cytoskeleton in action: lissencephaly, a neuronal migration disorder. Wiley Interdiscip Rev Dev Biol. 2(2), 229-245. doi: 10.1002/wdev.67.10.1002/wdev.67359379423495356Search in Google Scholar

5. Stutterd, C.A. & Leventer, R.J. (2014). Polymicrogyria: a common and heterogeneous malformation of cortical development. Am J Med Genet C Semin Med Genet. 166C(2), 227-239. doi: 10.1002/ajmg.c.31399.10.1002/ajmg.c.3139924888723Search in Google Scholar

eISSN:
1841-4036
Language:
English
Publication timeframe:
4 times per year
Journal Subjects:
Medicine, Clinical Medicine, other