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
- 16 Early Onset Early Onset Generalized Dystonia: DYT1
- 17 Early Onset Jerky Dystonia: An Uncommon Phenotype of DYT1
- 18 Early Onset Generalized Dystonia with Cranio-Cervical Involvement: DYT6
- 19 Autosomal Recessive Isolated Generalized Dystonia: DYT2
- 20 Dopa-Responsive Dystonia
- 21 A Complicated Dopa-Responsive Dystonia: Tyrosine Hydroxylase Deficiency
- 22 Early Onset Generalized Dystonia and Macrocephaly: Glutaric Aciduria Type 1
- 23 PKAN Misdiagnosed as ‘Progressive Delayed-Onset Postanoxic Dystonia’
- 24 Oromandibular Dystonia and Freezing of Gait: A Novel Presentation of Neuroferritinopathy
- 25 Generalized Dystonia with Oromandibular Involvement and Self-mutilations: Lesch–Nyhan Syndrome
- 26 Dystonia Complicated by Pyramidal Signs, Parkinsonism, and Cognitive Impairment: HSP11
- 27 H-ABC Syndrome
- 28 Tardive Dystonic Opisthotonus
- 29 Delayed Onset Dystonia after Lightning Strike
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
26 - Dystonia Complicated by Pyramidal Signs, Parkinsonism, and Cognitive Impairment: HSP11
from Section 2 - Dystonia
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
- 16 Early Onset Early Onset Generalized Dystonia: DYT1
- 17 Early Onset Jerky Dystonia: An Uncommon Phenotype of DYT1
- 18 Early Onset Generalized Dystonia with Cranio-Cervical Involvement: DYT6
- 19 Autosomal Recessive Isolated Generalized Dystonia: DYT2
- 20 Dopa-Responsive Dystonia
- 21 A Complicated Dopa-Responsive Dystonia: Tyrosine Hydroxylase Deficiency
- 22 Early Onset Generalized Dystonia and Macrocephaly: Glutaric Aciduria Type 1
- 23 PKAN Misdiagnosed as ‘Progressive Delayed-Onset Postanoxic Dystonia’
- 24 Oromandibular Dystonia and Freezing of Gait: A Novel Presentation of Neuroferritinopathy
- 25 Generalized Dystonia with Oromandibular Involvement and Self-mutilations: Lesch–Nyhan Syndrome
- 26 Dystonia Complicated by Pyramidal Signs, Parkinsonism, and Cognitive Impairment: HSP11
- 27 H-ABC Syndrome
- 28 Tardive Dystonic Opisthotonus
- 29 Delayed Onset Dystonia after Lightning Strike
- 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. 63 - 64Publisher: Cambridge University PressPrint publication year: 2017
References
Suggested Readings
Abdel Aleem, A, Abu-Shahba, N, Swistun, D, et al. Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum. Eur J Med Genet. 2011;54:82–5.Google ScholarPubMed
Paisán-Ruiz, C, Guevara, R, Federoff, M, et al. Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Mov Disord. 2010;25:1791–800.CrossRefGoogle ScholarPubMed
Schneider, SA, Mummery, CJ, Mehrabian, M, Houlden, H, Bain, PG. SPG11 presenting with tremor. Tremor Other Hyperkinet Mov (N Y). 2012;2. pii: tre-02-104-666-1.Google ScholarPubMed