830
Views
2
CrossRef citations to date
0
Altmetric
Research Article

Clinicopathological Analysis of Sturge–Weber Syndrome with Focal Cortical Dysplasia FCD IIIc

ORCID Icon, , , , , , & show all
Pages 545-556 | Received 15 Aug 2022, Accepted 17 Jan 2023, Published online: 03 Feb 2023

References

  • Silverstein M, Salvin J. Ocular manifestations of Sturge–Weber syndrome. Curr Opin Ophthalmol. 2019;30(5):301–5. doi:10.1097/ICU.0000000000000597.
  • Anbuselvan S, Venkatachalam P. Sturge–Weber syndrome and glaucoma. J Pharm Bioallied Sci. 2021;13(Suppl 2):S1765–S1768. doi:10.4103/jpbs.jpbs_354_21.
  • Wang DD, Blümcke I, Coras R, Zhou WJ, Lu DH, Gui QP, Hu JX, Zuo HC, Chen SY, Piao YS. Sturge–Weber syndrome is associated with cortical dysplasia ILAE type IIIc and excessive hypertrophic pyramidal neurons in brain resections for intractable epilepsy. Brain Pathol. 2015;25(3):248–55. doi:10.1111/bpa.12172.
  • Higueros E, Roe E, Granell E, Baselga E. Sturge–Weber syndrome: a review. Actas Dermosifiliogr. 2017;108(5):407–17. doi:10.1016/j.ad.2016.09.022.
  • Bianchi F, Auricchio AM, Battaglia DI, Chieffo DRP, Massimi L. Sturge–Weber syndrome: an update on the relevant issues for neurosurgeons. Childs Nerv Syst. 2020;36(10):2553–70. doi:10.1007/s00381-020-04695-3.
  • Pathak BD, Sharma S, Adhikari A, Simkhada N, Ghimire B, Aryal N. Sturge–Weber syndrome with bilateral Port-Wine stain. Case Rep Pediatr. 2022; 2022(4):2191465. doi:10.1155/2022/2191465.
  • Arinzechi EO, Ogunrin OA, Nwosu CM, Nwani PO, Enwereji KO, Asomugha LA, Dimkpa U. Seizure frequency and risk of cognitive impairment in people living with epilepsy in a sub-urban community in South Eastern Nigeria. J Clin Neurosci. 2019;59(1):98–105. doi:10.1016/j.jocn.2018.10.120.
  • Pedraza MI, de Lera M, Bos D, Calleja AI, Cortijo E, Gómez-Vicente B, Reyes J, Coco-Martín MB, Calonge T, Agulla J, et al. Brain Atrophy and the risk of futile endovascular reperfusion in acute ischemic stroke. Stroke. 2020;51(5):1514–21. doi:10.1161/STROKEAHA.119.028511.
  • Scheffer IE, Berkovic S, Capovilla G, Connolly MB, French J, Guilhoto L, Hirsch E, Jain S, Mathern GW, Moshé SL, et al. ILAE classification of the epilepsies: position paper of the ILAE Commission for Classification and Terminology. Epilepsia. 2017;58(4):512–21. doi:10.1111/epi.13709.
  • Swarup O, Waxmann A, Chu J, Vogrin S, Lai A, Laing J, Barker J, Seiderer L, Ignatiadis S, Plummer C, et al. Long-term mood, quality of life, and seizure freedom in intracranial EEG epilepsy surgery. Epilepsy Behav. 2021;123(10):108241. doi:10.1016/j.yebeh.2021.108241.
  • Fjaer R, Marciniak K, Sundnes O, Hjorthaug H, Sheng Y, Hammarström C, Sitek JC, Vigeland MD, Backe PH, Øye AM, et al. A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome. Hum Mol Genet. 2021;30(21):1919–31. doi:10.1093/hmg/ddab144.
  • Comi AM, Sahin M, Hammill A, Kaplan EH, Juhász C, North P, Ball KL, Levin AV, Cohen B, Morris J, 2015 Sturge-Weber Syndrome Research Workshop, et al. Leveraging a Sturge–Weber gene discovery: an agenda for future research. Pediatr Neurol. 2016;58(5):12–24. doi:10.1016/j.pediatrneurol.2015.11.009.
  • Dompmartin A, Vander Vleuten CJM, Dekeuleneer V, Duprez T, Revencu N, Désir J, Te Loo DMWM, Flucke U, Eijkelenboom A, Schultze Kool L, et al. GNA11-mutated Sturge–Weber Syndrome has distinct neurologic and dermatologic features. Eur J Neurol. 2022; 6(6):1–8. doi:10.1111/ene.15452.
  • Powell S, Fosi T, Sloneem J, Hawkins C, Richardson H, Aylett S. Neurological presentations and cognitive outcome in Sturge–Weber syndrome. Eur J Paediatr Neurol. 2021;34(9):21–32. doi:10.1016/j.ejpn.2021.07.005.
  • Miyata H, Kuwashige H, Hori T, Kubota Y, Pieper T, Coras R, Blümcke I, Yoshida Y. Variable histopathology features of neuronal dyslamination in the cerebral neocortex adjacent to epilepsy-associated vascular malformations suggest complex pathogenesis of focal cortical dysplasia ILAE type IIIc. Brain Pathol. 2022; 1(1):e13052. doi:10.1111/bpa.13052.