The paroxysmal dyskinesias

Journal of Neurology

Volumn 246, Issue 3, 1999, Pages 149-155

  Bhatia, Kailash P ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; ANTICONVULSIVE AGENT; CARBAMAZEPINE; CHOLINERGIC RECEPTOR; ION CHANNEL;

AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 20Q; CHROMOSOME 2Q; CLINICAL FEATURE; COFFEE; DYSKINESIA; DYSTONIA; EXERCISE; FATIGUE; FOOT; FRONTAL LOBE EPILEPSY; GENE MUTATION; GENETICS; HUMAN; MOTOR DYSFUNCTION; MULTIPLE SCLEROSIS; MUSCLE SPASM; PATHOPHYSIOLOGY; PRIORITY JOURNAL; RECEPTOR GENE; REVIEW; RUNNING; SANDIFFER SYNDROME; SEX RATIO; TEA; TORTICOLLIS; WALKING;

DYSTONIA; HUMANS; MOVEMENT DISORDERS; MUSCULAR DISEASES;

EID: 0032941645     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150050325     Document Type: Review

References (56)

1. 1. Mount LA, Reback S (1940) Familial paroxysmal choreoathetosis. Arch Neurol Psychiatry 44 : 841-847
2. 2. Forssman H (1961) Hereditary disorder characterized by attacks of muscular contractions, induced by alcohol amongst other factors. Acta Med Scand 170 : 517-533
3. 3. Lance JW (1963) Sporadic and familial varieties of tonic seizures. J Neurol Neurosurg Psychiatry 26 : 51-59
4. 4. Kertesz A (1967) Paroxysmal kinesigenic choreoathetosis. An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied. Neurology 17 : 680-690
5. 5. Kato M, Araki S (1969) Paroxysmal kinesigenic choreoathetosis. Report of a case relieved by carbamazepine. Arch Neurol 20 : 508-513
6. 6. Lance JW (1977) Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes. Ann Neurol 2 : 285-293
7. 7. Demirkirin M, Jankovic J (1995) Paroxysmal dyskinesias: clinical features and classification. Ann Neurol 38 : 571-579
8. 8. Fahn S (1994) The paroxysmal dyskinesias. In: Marsden CD, Fahn S (eds) Movement disorders 3. Butterworth-Heinemann, Oxford, pp 310-345
9. 9. Berger JR, Sheremata WA, Melamed E (1984) Paroxysmal dystonia as the initial manifestation of multiple sclerosis. Arch Neurol 41 : 747-750
10. 10. Matthews WB (1958) Tonic seizures in disseminated sclerosis. Brain 81 : 193-206
11. 11. Robin JJ (1977) Paroxysmal choreoathetosis following head injury. Ann Neurol 2:447-448
12. 12. Rosen JA (1964) Paroxysmal choreoathetosis. Associated with perinatal hypoxic encephalopathy. Arch Neurol 11 : 385-387
13. 13. Tabaee-Zadeh MJ, Frame B, Kapphahn K (1972) Kinesigenic choreoathetosis and idiopathic hypoparathyroidism. N Engl J Med 286 : 762-763
14. 14. Fishbeck KH, Layzer RB (1979) Paroxysmal choreoathetosis associated with thyrotoxicosis. Ann Neurol 6 : 453-454
15. 15. Adam AM, Orinda D (1986) Focal paroxysmal kinesigenic choreoathetosis preceding the development of Steele-Richardson-Olszweski syndrome. J Neurol Neurosurg Psychiatry 49 : 957-968
16. 16. Camac A, Greene P, Khandji A (1990) Paroxysmal kinesigenic dystonic choreoathetosis associated with a thalamic infarct. Mov Disord 5 : 235-238
17. 17. Newman RP, Kinkel WR (1984) Paroxysmal choreoathetosis due to hypoglycemia. Arch Neurol 41 : 341-342
18. 18. Clark JD, Pahwa R, Koller C, Morales D (1995) Diabetes mellitus presenting as a paroxysmal kinesigenic dystonic choreoathetosis. Mov Disord 10 : 353-355
19. 19. Lishman WA, Symonds CD, Whitty CW, Wilson RG (1962) Seizures induced by movement. Brain 85 : 93-108
20. 20. Kinast M, Erenberg G, Rothner AD (1980) Paroxysmal choreoathetosis, report of five cases and review of the literature. Pediatrics 65 : 74-77
21. 21. Falconer M, Driver M, Serafetinides E (1963) Seizures induced by movement: report of case relieved by operation. J Neurol Neurosurg Psychiatry 26 : 300-307
22. 22. Nardocci N, Lamperti E, Rumi V, Angelini L (1989) Typical and atypical forms of paroxysmal choreoathetosis. Dev Med Child Neurol 31 : 670-674
23. 23. Franssen H, Fortgens C, Wattendorff AE, Van Woerom TCAM (1983) Paroxysmal kinesigenic choreoathetosis and abnormal contingent negative variation. A case report. Arch Neurol 40 : 381-385
24. 24. Brunt ERP, Van Weerden TW (1990) Familial paroxysmal kinesigenic ataxia and continuous myokimia. Brain 113 : 1361-1382
25. 25. Griggs RC, Moxley RT III, Lafralane RA, McQuillen J (1978) Hereditary paroxysmal ataxia, response to acetazolamide. Neurology 28 : 1259-1264
26. 26. Browne DL, Gancher ST, Nutt JG, Brunt ER, Smith EA, Kramer P, Litt M (1994) Episodic ataxia myokimia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nat Genet 8 : 136-140
27. 27. Vahedi K, Joutel A, Van Vogaert P, Ducros A, Maciazeck J, Bach JF, Bousser MG, Tournier-Lasserve E (1995) A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19. Ann Neurol 37 : 289-293
28. 28. Ptacek LJ, Tawil R, Griggs RC, Meola G, McManis P, Barohn RJ, Mendell JR, et al (1994) Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis. Neurology 44 : 1500-1503
29. 29. Jurkat-Rott K, Lehmann-Horn F, Elbaz A, Heine R, Gregg RG, Hogan K, Powers PA, et al (1994) A calcium-channel mutation causing hypokalemic periodic paralysis. Hum Mol Genet 3 : 1415-1419
30. 30. Kramer Pl, Yue Q, Gansher ST, et al (1995) A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cm region on chromosome 19p. Am J Hum Genet 57 : 182-185
31. 2+ channel gene CACNLIA4. Cell 87 : 543-552
32. 32. Plant GT, Williams AC, Early CJ, Marsden CD (1984) Familial paroxysmal dystonia induced by exercise. J Neurol Neurosurg Psychiatry 47 : 275-279
33. 33. Wali GM (1992) Paroxysmal hemidystonia induced by prolonged exercise and cold. J Neurol Neurosurg Psychiatry 55 : 236-237
34. 34. Bhatia KP, Soland VL, Bhatt MH, Quinn NP, Marsden CD (1997) Paroxysmal exercise-induced dystonia: eight new sporadic cases and a review of the literature. Mov Disord 12 : 1007-1012
35. 35. Segawa M, Hosaka A, Miyawaga F, Nomura Y, Imai H (1976) Hereditary progressive dystonia with marked diurnal fluctuations. Adv Neurol 14 : 215-233
36. 36. Bressman SB, Fahn S (1988) Burke RE. Paroxysmal non-kinesigenic dystonia. Adv Neurol 50 : 403-413
37. 37. Byrne E, White O, Cook M (1991) Familial dystonic choreoathetosis with myokimia; a sleep responsive disorder. J Neurol Neurosurg Psychiatry 54 : 1090-1092
38. 38. Wahnschaffe U, Fredow G, Heinz P, Losher W (1990) Neuropathological studies in a mutant hamster model of paroxysmal dystonia. Mov Disord 5 : 286-293
39. 39. Sethi KD, Hess DC, Huffnagle VH, Adams RJ (1992) Acetazolamide treatment of paroxysmal dystonia in central demyelinating disease. Neurology 42 : 919-921
40. 40. Lee MS, Marsden CD (1994) Movement disorders following lesions of the thalamus or subthalamic region. Mov Disord 9 : 493-507
41. 41. Drake M Jr, Jackson RD, Miller CA (1986) Paroxysmal choreoathetosis after closed head injury. J Neurol Neurosurg Psychiatry 49 : 837-843
42. 42. Soffer D, Licht A, Yaar L, Abramsky O (1977) Paroxysmal choreoathetosis as a presenting symptom in idiopathic hypoparathyroidism. J Neurol Neurosurg Psychiatry 40 : 692-694
43. 43. Micheli F, Fernandez Pardal M, Casas Parera I, Giannaula R (1986) Sporadic paroxysmal dystonic choreoathetosis associated with basal ganglia calcifications. Ann Neurol 20 : 750
44. 44. Nath A, Jankovic J, Pettigrew LC (1987) Movement disorders and AIDS. Neurology 37 : 37-41
45. 45. Fouad GT, Sevidei S, Durcan S, Bertini E, Ptacek LJ (1996) A gene for familial dyskinesia (FPD1) maps to chromosome 2q. Am J Hum Genet 59 : 135-139
46. 46. Fink JK, Rainer S, Wilkowski J, et al (1996) Paroxysmal dystonic choreoathetosis. Tight linkage to chromosome 2q. Am J Hum Genet 59 : 140-145
47. 47. Lugaresi E, Cirignotti F (1981) Hypnogenic paroxysmal dystonia: epileptic seizure or a new syndrome. Sleep 4 : 129-138
48. 48. Lee BI, Lesser RP, Pippenger CE, et al (1985) Familial paroxysmal hypnogenic dystonia. Neurology 35 : 1357-1360
49. 49. Meierkord H, Fish DR, Smith SJM, Scott CA, Shorvon SD, Marsden CD (1992) Is nocturnal dystonia a form of frontal lobe epilepsy? Mov Disord 7 : 38-42
50. 50. Tinuper P, Cerullo A, Cirignotti F, Cortelli P, Lugaresi E, Montagna P (1990) Nocturnal paroxysmal dystonia with short lasting attacks: three cases with evidence for an epileptic frontal lobe origin of seizures. Epilepsia 31 : 549-556
51. 51. Scheffer IE, Bhatia KP, Lopes-Cendes I, et al (1995) Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder. Brain 118 : 61-73
52. 52. Scheffer IE, Bhatia KP, Lopes-Cendes I, et al (1994) Autosomal dominant frontal lobe epilepsy misdiagnosed as a sleep disorder. Lancet 343 : 515-517
53. 53. Phillips HA, Scheffer IE, Berkovic SF, Holloway GE, Sutherland GR, Mulley JC (1995) Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2. Nat Genet 10 : 117-118
54. 54. Tranchant C, Bhatia KP, Marsden CD (1995) Movement disorders in multiple sclerosis. Mov Disord 10 : 418-423
55. 55. Kinsbourne M (1964) Hiatus hernia with contortions of the neck. Lancet 1 : 1058-1061
56. 56. Auburger G, Ratzlaff T, Lunkes A, Nelles HW, Leube B, Binkofski F, Kugel H, et al (1966) A gene for autososmal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromososme 1p, probably within 2 cM between D1S443 and D1S197. Genomics 31 : 90-94