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
- 1 Parkinson’s Disease
- 2 Nonmotor Parkinson’s Disease
- 3 Isolated Lower Limb Dystonia at Onset of Parkin Disease
- 4 Parkinson’s Disease Associated with SNCA Mutations
- 5 PSP: Steele-Richardson-Olszewski Syndrome
- 6 PSP-Parkinsonism
- 7 Corticobasal Degeneration
- 8 MSA – Parkinsonian Variant
- 9 Prominent Freezing of Gait and Speech Disturbances Due to Fahr Disease
- 10 A (Familial) PSP Look-Alike: Perry Syndrome
- 11 Parkinsonian Syndrome and Sunflower Cataracts: Wilson’s Disease
- 12 Classic PD-Like Rest Tremor in FTDP-17 Due to a MAPT Mutation
- 13 PSP Look-Alike due to CADASIL
- 14 Very Early Onset Parkinsonism: Juvenile HD
- 15 Parkinsonism Due to CSF1R Mutation
- Section 2 Dystonia
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
13 - PSP Look-Alike due to CADASIL
from Section 1 - Parkinsonism
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
- 1 Parkinson’s Disease
- 2 Nonmotor Parkinson’s Disease
- 3 Isolated Lower Limb Dystonia at Onset of Parkin Disease
- 4 Parkinson’s Disease Associated with SNCA Mutations
- 5 PSP: Steele-Richardson-Olszewski Syndrome
- 6 PSP-Parkinsonism
- 7 Corticobasal Degeneration
- 8 MSA – Parkinsonian Variant
- 9 Prominent Freezing of Gait and Speech Disturbances Due to Fahr Disease
- 10 A (Familial) PSP Look-Alike: Perry Syndrome
- 11 Parkinsonian Syndrome and Sunflower Cataracts: Wilson’s Disease
- 12 Classic PD-Like Rest Tremor in FTDP-17 Due to a MAPT Mutation
- 13 PSP Look-Alike due to CADASIL
- 14 Very Early Onset Parkinsonism: Juvenile HD
- 15 Parkinsonism Due to CSF1R Mutation
- Section 2 Dystonia
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
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- Case Studies in Movement DisordersCommon and Uncommon Presentations, pp. 31 - 32Publisher: Cambridge University PressPrint publication year: 2017
References
Suggested Readings
Moccia, M, Mosca, L, Erro, R, et al. Hypomorphic NOTCH3 mutation in an Italian family with CADASIL features. Neurobiol Aging. 2015;36(1):547.e5–11.Google Scholar
Ragno, M, Berbellini, A, Cacchiò, G, et al. Parkinsonism is a late, not rare, feature of CADASIL. Stroke. 2013;44(4):1147–9.CrossRefGoogle Scholar
Stamelou, M, Quinn, NP, Bhatia, KP. ‘Atypical’ atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy. Mov Disord. 2013;28(9):1184–99.CrossRefGoogle ScholarPubMed