Case Studies in Movement Disorders

Table of Contents

• 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.
Show more