Tom 17, Nr 3 (2021)
Obrazy w medycynie
Opublikowany online: 2021-10-16
Wyświetlenia strony
3342
Wyświetlenia/pobrania artykułu
127
Polimikrogyria z towarzyszącą malrotacją hipokampa jako przyczyna padaczki
Pol. Przegl. Neurol 2021;17(3):138-140.
Streszczenie
Brak
Referencje
- Barkovich AJ, Guerrini R, Kuzniecky RI, et al. A developmental and genetic classification for malformations of cortical development: update 2012. Brain. 2012; 135(Pt 5): 1348–1369.
- Shain C, Ramgopal S, Fallil Z, et al. EPGP Investigators. Polymicrogyria-associated epilepsy: a multicenter phenotypic study from the Epilepsy Phenome/Genome Project. Epilepsia. 2013; 54(8): 1368–1375.
- Robin NH, Taylor CJ, McDonald-McGinn DM, et al. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation. Am J Med Genet A. 2006; 140(22): 2416–2425.
- De Ciantis A, Barkovich AJ, Cosottini M, et al. Ultra-high-field MR imaging in polymicrogyria and epilepsy. AJNR Am J Neuroradiol. 2015; 36(2): 309–316.
- Andrade DM, Krings T, Chow EWC, et al. Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. Can J Neurol Sci. 2013; 40(5): 652–656.
- Fu TY, Ho CR, Lin CH, et al. Hippocampal malrotation: a genetic developmental anomaly related to epilepsy? Brain Sci. 2021; 11(4).
- Mutti C, Riccò M, Bartolini Y, et al. Incomplete hippocampal inversion and epilepsy: a systematic review and meta-analysis. Epilepsia. 2021; 62(2): 383–396.
- Sato N, Hatakeyama S, Shimizu N, et al. MR evaluation of the hippocampus in patients with congenital malformations of the brain. Am J Neuroradiol. 2001; 22: 389–393.
- Caciagli L, Wandschneider B, Xiao F, et al. Abnormal hippocampal structure and function in juvenile myoclonic epilepsy and unaffected siblings. Brain. 2019; 142(9): 2670–2687.
