Kailash P Bhatia, Roberto Erro, Maria Stamelou

Case Studies in Movement Disorders

Common and Uncommon Presentations

• Broschiertes Buch

Produktbeschreibung

A thorough collection of movement disorders cases, each discussed by international experts and accompanied by illustrative video content.

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Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.

Produktdetails

• Verlag: Cambridge University Press
• Seitenzahl: 170
• Erscheinungstermin: 2. Juni 2017
• Englisch
• Abmessung: 246mm x 187mm x 12mm
• Gewicht: 408g
• ISBN-13: 9781107472426
• ISBN-10: 1107472423
• Artikelnr.: 48503157

Autorenporträt

Kailash Bhatia is a Professor of Clinical Neurology in the Sobell Department of Motor Neuroscience and Movement Disorders at the Institute of Neurology, University College London and an Honorary Consultant Neurologist at the affiliated National Hospital for Neurology, London.

Inhaltsangabe

List of contributors
List of abbreviations
Section 1. Parkinsonism: 1. Parkinson disease
2. Nonmotor Parkinson disease
3. Isolated lower limb dystonia at onset of Parkin disease
4. Parkinson's disease associated with SCNA mutations
5. 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
11. Parkinsonian syndrome and sunflower cataracts: Wilson's disease
12. Classic PD-like rest tremor in FTDP-17 due to a MAPT mutation
13. Progressive parkinsonism with falls and supranuclear gaze palsy
14. Very early onset parkinsonism
15. Parkinsonism due to CSF1R mutation
Section 2. Dystonia: 16. 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. Dystonic opisthotonus
29. Delayed-onset dystonia after lightning strike
Section 3. Tics: 30. Gilles de la Tourette syndrome
31. Secondary tic disorders: Huntington disease
32. Multiple hyperkinesias: tics and paroxysmal kinesigenic dyskinesia
33. Functional tic disorders
Section 4. Chorea: 34. Huntington disease
35. Generalized chorea with oromandibular involvement and tongue biting
36. A Huntington disease 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
41. Another cause of benign hereditary chorea
Section 5. Tremor: 42. Essential tremor
43. Rest tremor and scans without evidence of dopaminergic deficit (SWEDD)
44. Neuropathic tremor
45. A treatable disorder misdiagnosed as ET
46. Thalamic tremor
47. Shaking on standing: orthostatic tremor
48. Palatal tremor
49. Dystonic tremor and progressive ataxia
50. Bilateral Holmes tremor in multiple sclerosis
51. Primary writing tremor
Section 6. Myoclonus: 52. A case of 'essential' myoclonus
53. Ramsey Hunt syndrome and Unverricht-Lundborg disease
54. North Sea myoclonus due to GOSR2 mutations
55. Ramsay Hunt syndrome and coeliac disease
56. Asymmetric myoclonus and apraxia: corticobasal syndromep
57. Rapidly progressive cognitive regression and myoclonus
58. Familial cortical 'tremor'
59. Prominent myoclonus and parkinsonism
60. Axial myoclonus of uncertain origin
Section 7. Ataxia: 61. Slowly progressive unsteadiness and double vision
62. Cerebellar ataxia with urinary incontinence: MSA-C
63. Progressive ataxia, tremor, autonomic dysfunction and cognitive impairment
64. Sensory ataxic neuropathy with dysarthria and ophthalmoparesis (SANDO) syndrome
65. Ataxia telangiectasia without ataxia
66. Anti-Yo related ataxia misdiagnosed as multiple system atrophy
67. Late onset spinocerebellar ataxia
68. Ataxia with splenomegaly: Niemann-Pick disease type C.