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Chapter 6 - Familial Electro-clinical Syndromes and Epilepsies in Adolescence to Adulthood

Published online by Cambridge University Press:  11 October 2019

By
Elie Abdelnour ,
Monisha Sachdev  and
Mohamad Mikati
Edited by
Vibhangini S. Wasade  and
Marianna V. Spanaki
Vibhangini S. Wasade
Affiliation:
Henry Ford Medical Group HFHS, Michigan
Marianna V. Spanaki
Affiliation:
Wayne State University, Michigan
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Summary

Autosomal dominant epilepsy with auditory features (ADEAF), also referred to as autosomal dominant lateral temporal epilepsy (ADLTE), is one type of familial temporal lobe epilepsy.

Type
Chapter
Information
Understanding Epilepsy
A Study Guide for the Boards
 , pp. 110 - 126
Publisher: Cambridge University Press
Print publication year: 2019

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References

Klein, KM, Pendziwiat, M, Cohen, R, et al. Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia. J Neurol. 2016;263(1):11–16.CrossRefGoogle ScholarPubMed
Boillot, M, Huneau, C, Marsan, E, et al. Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures. Brain. 2014;137(Pt 11):2984–2996.CrossRefGoogle ScholarPubMed
Michelucci, R, Pasini, E, Nobile, C. Lateral temporal lobe epilepsies: clinical and genetic features. Epilepsia. 2009;50(Suppl 5):52–54.CrossRefGoogle ScholarPubMed
Michelucci, R, Pulitano, P, Di Bonaventura, C, et al. The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations. Epilepsy Behav. 2017;68:103–107.CrossRefGoogle ScholarPubMed
Picard, F, Baulac, S, Kahane, P, et al. Dominant partial epilepsies: a clinical, electrophysiological and genetic study of 19 European families. Brain. 2000;123(Pt 6):1247–1262.CrossRefGoogle Scholar
Picard, F, Bruel, D, Servent, D, et al. Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study. Brain. 2006;129(Pt 8):2047–2060.CrossRefGoogle ScholarPubMed
Heron, SE, Smith, KR, Bahlo, M, et al. Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy. Nat Genet. 2012;44(11):1188–1190.CrossRefGoogle ScholarPubMed
Mikati, MA, Jiang, YH, Carboni, M, et al. Quinidine in the treatment of KCNT1-positive epilepsies. Ann Neurol. 2015;78(6):995–999.CrossRefGoogle ScholarPubMed
Carreno, M, Garcia-Alvarez, D, Maestro, I, et al. Malignant autosomal dominant frontal lobe epilepsy with repeated episodes of status epilepticus: successful treatment with vagal nerve stimulation. Epileptic Disord. 2010;12(2):155–158.Google ScholarPubMed
Weckhuysen, S, Marsan, E, Lambrecq, V, et al. Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia. Epilepsia. 2016;57(6):994–1003.CrossRefGoogle ScholarPubMed
Leventer, RJ, Jansen, FE, Mandelstam, SA, et al. Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibility. Epilepsia. 2014;55(3):e22–26.CrossRefGoogle ScholarPubMed
Ishida, S, Picard, F, Rudolf, G, et al. Mutations of DEPDC5 cause autosomal dominant focal epilepsies. Nat Genet. 2013;45(5):552–555.CrossRefGoogle ScholarPubMed
Jermakowicz, WJ, Kanner, AM, Sur, S, et al. Laser thermal ablation for mesiotemporal epilepsy: analysis of ablation volumes and trajectories. Epilepsia. 2017;58(5):801–810.CrossRefGoogle ScholarPubMed
Beghi, M, Beghi, E, Cornaggia, CM, Gobbi, G. Idiopathic generalized epilepsies of adolescence. Epilepsia. 2006;47(Suppl 2):107–110.CrossRefGoogle ScholarPubMed
Japaridze, G, Kasradze, S, Lomidze, G, et al. Focal EEG features and therapeutic response in patients with juvenile absence and myoclonic epilepsy. Clin Neurophysiol. 2016;127(2):1182–1187.CrossRefGoogle ScholarPubMed
Seneviratne, U, Cook, M, D’Souza, W. Focal abnormalities in idiopathic generalized epilepsy: a critical review of the literature. Epilepsia. 2014;55(8):1157–1169.CrossRefGoogle ScholarPubMed
Tondelli, M, Vaudano, AE, Ruggieri, A, Meletti, S. Cortical and subcortical brain alterations in juvenile absence epilepsy. Neuroimage Clin. 2016;12:306–311.CrossRefGoogle ScholarPubMed
Bergey, GK. Evidence-based treatment of idiopathic generalized epilepsies with new antiepileptic drugs. Epilepsia. 2005;46(Suppl 9):161–168.CrossRefGoogle ScholarPubMed
Anastasopoulou, S, Kurth, F, Luders, E, Savic, I. Generalized epilepsy syndromes and callosal thickness: differential effects between patients with juvenile myoclonic epilepsy and those with generalized tonic-clonic seizures alone. Epilepsy Res. 2017;129:74–78.CrossRefGoogle ScholarPubMed
Paulus, FM, Krach, S, Blanke, M, et al. Fronto-insula network activity explains emotional dysfunctions in juvenile myoclonic epilepsy: combined evidence from pupillometry and fMRI. Cortex. 2015;65:219–231.CrossRefGoogle ScholarPubMed
Aydin-Ozemir, Z, Terzibasioglu, E, Altindag, E, Sencer, S, Baykan, B. Magnetic resonance spectroscopy findings in photosensitive idiopathic generalized epilepsy. Clin EEG Neurosci. 2010;41(1):42–49.CrossRefGoogle ScholarPubMed
Kim, SH, Lim, SC, Kim, W, et al. Extrafrontal structural changes in juvenile myoclonic epilepsy: a topographic analysis of combined structural and microstructural brain imaging. Seizure. 2015;30:124–131.CrossRefGoogle ScholarPubMed
Yacubian, EM. Juvenile myoclonic epilepsy: challenges on its 60th anniversary. Seizure. 2017;44:48–52.CrossRefGoogle ScholarPubMed
Uchida, CG, de Carvalho, KC, Guaranha, MS, et al. Phenotyping juvenile myoclonic epilepsy. Praxis induction as a biomarker of unfavorable prognosis. Seizure. 2015;32:62–68.CrossRefGoogle ScholarPubMed
Iivanainen, M, Himberg, JJ. Valproate and clonazepam in the treatment of severe progressive myoclonus epilepsy. Arch Neurol. 1982;39(4):236–238.CrossRefGoogle ScholarPubMed
Koskenkorva, P, Khyuppenen, J, Niskanen, E, et al. Motor cortex and thalamic atrophy in Unverricht-Lundborg disease: voxel-based morphometric study. Neurology. 2009;73(8):606–611.CrossRefGoogle ScholarPubMed
Andrade, DM, del Campo, JM, Moro, E, Minassian, BA, Wennberg, RA. Nonepileptic visual hallucinations in Lafora disease. Neurology.

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