Paroxysmal dyskinesias in childhood

Pediatric Neurology

Volumn 28, Issue 3, 2003, Pages 168-172

  Zorzi, Giovanna ^a   Conti, Chiara ^a   Erba, Anna ^a   Granata, Tiziana ^a   Angelini, Lucia ^a   Nardocci, Nardo ^a  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAZOLAMIDE; ANTICONVULSIVE AGENT; CARBAMAZEPINE; CLONAZEPAM; ION CHANNEL; LEVODOPA; PHENYTOIN; VALPROIC ACID;

ADOLESCENT; ARTICLE; BASAL GANGLION; BRAIN DISEASE; CEREBRAL PALSY; CHIARI FROMMEL SYNDROME; CHILD; CHROMOSOME 16; CHROMOSOME MAP; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE CLASSIFICATION; DRUG EFFICACY; DYSKINESIA; EXERCISE; FAMILIAL DISEASE; FAMILY HISTORY; FEMALE; GENETIC ANALYSIS; HUMAN; HYPOTHESIS; IDIOPATHIC DISEASE; MALE; NERVE INJURY; ONSET AGE; PRIORITY JOURNAL; ROLANDIC EPILEPSY; STROKE; TREATMENT OUTCOME;

EID: 0038288675     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(02)00512-X     Document Type: Article

References (35)

1. Mount L.A., Reback S. Familial paroxysmal choreoathetosis. Arch Neurol Psychiatry. 44:1940;841-847.
2. Demirkiran M., Jankovic J. Paroxysmal dyskinesias Clinical features and classification . Ann Neurol. 38:1995;571-579.
3. Lugaresi E., Cirignotta F., Montagna P. Nocturnal paroxysmal dystonia. J Neurol Neurosurg Psychiatry. 49:1986;375-380.
4. Provini F., Plazzi G., Tinuper P., Vandi S., Lugaresi E., Montagna P. Nocturnal frontal lobe epilepsy A clinical and polygraphic overview over 100 consecutive cases . Brain. 122:1999;1017-1031.
5. Steinlein O.K., Mulley J.C., Propping P., et al. A missense mutation in the neuronal nicotinic acetylcholine receptor a4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy. Nat Genet. 11:1995;201-203.
6. Phillips H.A., Favre I., Kirkpatrick M., et al. CHRNB2 is the second acetylcholine receptor associated with a dominant nocturnal frontal lobe epilepsy. Am J Hum Genet. 68:2001;225-231.
7. Marsden C.D. Paroxysmal choreoathetosis. Adv Neurol. 70:1996;467-470.
8. Bathia K.B. The paroxysmal dyskinesias. J Neurol. 246:1999;149-155.
9. Fouad G.T., Servidei S., Durcan S., Bertini E., Ptàcek L.J. A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q. Am J Hum Genet. 59:1996;135-139.
10. Fink J.K., Hedera P., Mathay J.G., Albin R.L. Paroxysmal dystonic choreoathetosis linked to chromosome 2q Clinical analysis and proposed pathophysiology . Neurology. 49:1997;177-183.
11. Tomita H., Nagamitsu S., Wakui K., et al. Paroxysmal kinesigenic locus maps to chromosome 16p11.2-q12.1. Am J Hum Genet. 65:1999;1688-1697.
12. Valente E.M., Spacey S.D., Wali G.M., et al. A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give raise to paroxysmal disorders on human chromosome 16. Brain. 123:2000;2040-2045.
13. Bennet L.B., Roach E.S., Bowcock A.M. A locus for paroxysmal kinesigenic dyskinesias maps to human chromosome 16. Neurology. 54:2000;125-130.
14. Guerrini R., Bonanni P., Nardocci N., et al. Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp Delineation of the syndrome and gene mapping to chromosome 16p12-11.2 . Ann Neurol. 45:1999;344-352.
15. Lance J.W. Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes. Ann Neurol. 2:1977;285-293.
16. Hwang W.J., Lu C.S., Tsai J.J. Clinical manifestations of 20 Taiwanese patients with paroxysmal kinesigenic dyskinesia. Acta Neurol Scand. 98:1998;340-345.
17. Houser M., Soland V.L., Bathia K.P., Quinn N.P., Marsden C.D. Paroxysmal kinesigenic choreoathetosis A report of 26 patients . J Neurol. 246:1999;120-126.
18. Fahn S. The paroxysmal dyskinesias. Marsden C.D., Fahn S. Movement disorders. 1994;310-345 Butterworth-Heinemann, Boston. vol 13.
19. Cosentino C., Torres L., Flores M., Cuba J.M. Paroxysmal kinesigenic dystonia and spinal cord lesion. Mov Disord. 11:1996;453-455.
20. Riley D.E. Paroxysmal kinesigenic dystonia associated with a medullary lesion. Mov Disord. 11:1996;738-740.
21. Bressman S.B., Fahn S., Burke R.E. Paroxysmal non-kinesigenic dystonia. Adv Neurol. 50:1988;403-413.
22. Bathia K.P., Soland V.L., Bhatt M.H., Quinn N.P., Marsden C.D. Paroxysmal exercise-induced dystonia Eight new sporadic cases and a review of the literature . Mov Disord. 12:1997;1007-1012.
23. Jung S.S., Chen K.M., Brody J.A. Paroxysmal choreoathetosis Report of Chinese cases . Neurology. 23:1973;749-755.
24. Goodenough D.J., Fariello R.G., Annis B.L., Chun R.W. Familial and acquired paroxysmal dyskinesias A proposed classification with delineation of clinical features . Arch Neurol. 35:1978;827-831.
25. Tan L.C., Tan A.K., Tjia H. Paroxysmal kinesigenic choreoathetosis in Singapore and its relation to epilepsy. Clin Neurol Neurosurg. 100:1998;187-192.
26. Guerrini R. Idiopathic epilepsy and paroxysmal dyskinesia. Epilepsia. 42:(Suppl 3):2001;36-41.
27. Hudgins R.L., Corbin K.B. An uncommon seizure disorder Familial paroxysmal choreoathetosis . Brain. 89:1966;199-204.
28. Szepetowski P., Rochette J., Berquin P., Piussan C., Lathrop G.M., Monaco A.P. Familial infantile convulsions and paroxysmal choreoathetosis A new neurological syndrome linked to the pericentromeric region of human chromosome 16 . Am J Hum Genet. 61:1997;889-898.
29. Swoboda K.J., Soong B.W., McKenna C., et al. Paroxysmal kinesigenic dyskinesias and infantile convulsions Clinical and linkage studies . Neurology. 55:2000;224-230.
30. Hattori H., Fujii T., Nigami H., Higuchi Y., Tsuji M., Hamada Y. Co-segregation of benign infantile convulsions and paroxysmal kinesigenic choreoathetosis. Brain Dev. 22:2000;432-435.
31. Hattori H., Yorifuji T. Infantile convulsions and paroxysmal choreoathetosis in a patient with idiopathic hypoparathyroidism. Brain Dev. 22:2000;449-450.
32. Perniola T., Margari L., De Iaco M.G., et al. Familial paroxysmal exercise-induced dyskinesias, epilepsy and mental retardation in a family with autosomal dominant inheritance. Mov Disord. 16:2001;724-730.
33. Margari L., Perniola T., Illiceto G., et al. Familial exercise-induced dyskinesia and benign epilepsy a clinical and neurophysiological study of an uncommon disorder . Neurol Sci. 21:2000;165-172.
34. Singh R., Macdonnell R.A., Scheffer I.E., Crossland K.M., Berkovic S.F. Epilepsy and paroxysmal movement disorder in families Evidence for shared mechanisms . Epileptic Disord. 1:1999;93-99.
35. Wood N.W., Kinton L., Hanna M.G. Genetics of the overlap between epilepsy and movement disorder. Guerrini R., Aicardi J., Andermann F., Hallet M. Epilepsy and movement disorders. 2002;451-464 Cambridge University Press, Cambridge.