Book contents
- Case Studies in Movement Disorders
- Case Studies in Movement Disorders
- Copyright page
- Contents
- Video Captions
- Contributors
- Preface
- Previously Published Cases
- Abbreviations
- Section 1 Parkinsonism
- Section 2 Dystonia
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- 52 A Case of Myoclonus-Dystonia
- 53 Progressive Myoclonic Ataxia and Unverricht-Lundborg Disease
- 54 North Sea Myoclonus Due to GOSR2 Mutations
- 55 Progressive Myoclonic Ataxia and Coeliac Disease
- 56 Asymmetric Myoclonus and Apraxia: Corticobasal Syndrome
- 57 Rapidly Progressive Cognitive Regression and Myoclonus: New Variant CJD
- 58 Familial Cortical ‘Tremor’
- 59 Prominent Myoclonus and Parkinsonism in MSA
- 60 Functional Axial Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
58 - Familial Cortical ‘Tremor’
from Section 6 - Myoclonus
Published online by Cambridge University Press: 04 July 2017
Book contents
- Case Studies in Movement Disorders
- Case Studies in Movement Disorders
- Copyright page
- Contents
- Video Captions
- Contributors
- Preface
- Previously Published Cases
- Abbreviations
- Section 1 Parkinsonism
- Section 2 Dystonia
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- 52 A Case of Myoclonus-Dystonia
- 53 Progressive Myoclonic Ataxia and Unverricht-Lundborg Disease
- 54 North Sea Myoclonus Due to GOSR2 Mutations
- 55 Progressive Myoclonic Ataxia and Coeliac Disease
- 56 Asymmetric Myoclonus and Apraxia: Corticobasal Syndrome
- 57 Rapidly Progressive Cognitive Regression and Myoclonus: New Variant CJD
- 58 Familial Cortical ‘Tremor’
- 59 Prominent Myoclonus and Parkinsonism in MSA
- 60 Functional Axial Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
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- Case Studies in Movement DisordersCommon and Uncommon Presentations, pp. 129 - 130Publisher: Cambridge University PressPrint publication year: 2017
References
Suggested Readings
Cen, Z, Huang, C, Yin, H, et al. Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy. Mov Disord. 2016;31:1704–1710.Google Scholar
Gao, L, Li, L, Ye, J, et al. Identification of a novel mutation in PLA2G6 gene in a Chinese pedigree with familial cortical myoclonic tremor with epilepsy. Seizure. 2016;41:81–5.CrossRefGoogle Scholar
Martí-Massó, JF, Bergareche, A, Makarov, V, et al. The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism. J Mol Med (Berl). 2013;91:1399–406.CrossRefGoogle Scholar
Stogmann, E, Reinthaler, E, Eltawil, S, et al. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Brain. 2013;136:1155–60.Google Scholar
van Rootselaar, AF, van Schaik, IN, van den Maagdenberg, AM, et al. Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features. Mov Disord. 2005;20:665–73.Google Scholar