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
- 34 Chorea and Cognitive Difficulty: HD
- 35 Generalized Chorea with Oromandibular Involvement and Tongue Biting: Chorea-acanthocytosis
- 36 A HD Look-Alike: SCA17
- 37 A Newly Recognized HD-Phenocopy Associated with C9orf72 Expansion
- 38 Persistent Chorea Due to Anticholinergics in DYT6
- 39 Dyskinesia without Levodopa: Long-Term Follow-Up of Mesencephalic Transplant in PD
- 40 Benign Hereditary Chorea due to TITF-1 Mutations
- 41 Another Cause of Benign Hereditary Chorea due to ADCY5 Mutations
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
41 - Another Cause of Benign Hereditary Chorea due to ADCY5 Mutations
from Section 4 - Chorea
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
- 34 Chorea and Cognitive Difficulty: HD
- 35 Generalized Chorea with Oromandibular Involvement and Tongue Biting: Chorea-acanthocytosis
- 36 A HD Look-Alike: SCA17
- 37 A Newly Recognized HD-Phenocopy Associated with C9orf72 Expansion
- 38 Persistent Chorea Due to Anticholinergics in DYT6
- 39 Dyskinesia without Levodopa: Long-Term Follow-Up of Mesencephalic Transplant in PD
- 40 Benign Hereditary Chorea due to TITF-1 Mutations
- 41 Another Cause of Benign Hereditary Chorea due to ADCY5 Mutations
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
Summary
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- Case Studies in Movement DisordersCommon and Uncommon Presentations, pp. 95 - 96Publisher: Cambridge University PressPrint publication year: 2017
References
Suggested Readings
Carapito, R, Paul, N, Untrau, M, et al. A De Novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia. Mov Disord. 2015;30:423–7.CrossRefGoogle Scholar
Chen, DH, Méneret, A, Friedman, JR., et al. ADCY5-related dyskinesia: broader spectrum and genotype-phenotype correlations. Neurology. 2015;85:2026–3.CrossRefGoogle ScholarPubMed
Mencacci, NE, Erro, R, Wiethoff, S. et al. ADCY5 mutations are another cause of benign hereditary chorea. Neurology. 2015;85:80–8.CrossRefGoogle ScholarPubMed