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
16 - Early Onset Early Onset Generalized Dystonia: DYT1
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
Summary
A summary is not available for this content so a preview has been provided. Please use the Get access link above for information on how to access this content.
- Type
- Chapter
- Information
- Case Studies in Movement DisordersCommon and Uncommon Presentations, pp. 39 - 41Publisher: Cambridge University PressPrint publication year: 2017
References
Suggested Readings
Bressman, SB, Sabatti, C, Raymond, D, et al. The DYT1 phenotype and guidelines for diagnostic testing. Neurology. 2000;54:1746–52.CrossRefGoogle ScholarPubMed
Valente, EM, Warner, TT, Jarman, PR, et al. The role of DYT1 in primary torsion dystonia in Europe. Brain. 1998;121:2335–9.CrossRefGoogle ScholarPubMed