Psychogenic paroxysmal movement disorders - Clinical features anddiagnostic clues

Parkinsonism and Related Disorders

Volumn 20, Issue 1, 2014, Pages 41-46

  Ganos, Christos ^a,b   Aguirregomozcorta, Maria ^a   Batla, Amit ^a   Stamelou, Maria ^a,c,d   Schwingenschuh, Petra ^a,e   Münchau, Alexander ^f   Edwards, Mark J ^a   Bhatia, Kailash P ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^c UNIVERSITY OF ATHENS   (Greece)

^d PHILIPPS UNIVERSITY MARBURG   (Germany)

^e MEDICAL UNIVERSITY OF GRAZ   (Austria)

^f UNIVERSITY OF LÜBECK   (Germany)

Author keywords

Paroxysmal dyskinesias; PED; PKD; PNKD; Psychogenic movement disorders

Indexed keywords

ARTICLE; CLINICAL FEATURE; COMORBIDITY; DISEASE DURATION; DYSTONIA; EMOTIONAL STRESS; EMOTIONALITY; FEMALE; HUMAN; LIFE EVENT; MAJOR CLINICAL STUDY; MALE; MOTOR DYSFUNCTION; ONSET AGE; PHENOMENOLOGY; PRIORITY JOURNAL; PSYCHOGENIC PAROXYSMAL MOVEMENT DISORDER; TREATMENT RESPONSE;

PAROXYSMAL DYSKINESIAS; PED; PKD; PNKD; PSYCHOGENIC MOVEMENT DISORDERS;

ADOLESCENT; ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; CHOREA; ELECTROENCEPHALOGRAPHY; FEMALE; HUMANS; MALE; MIDDLE AGED; RETROSPECTIVE STUDIES; SOMATOFORM DISORDERS; VIDEO RECORDING; YOUNG ADULT;

EID: 84892811055     PISSN: 13538020     EISSN: 18735126     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2013.09.012     Document Type: Article

References (33)

1. Bhatia K.P. Paroxysmal dyskinesias. Mov Disord 2011, 26:1157-1165.
2. Mount L.A., Reback S. Familial paroxysmal choreoathetosis - preliminary report on a hitherto undescribed clinical syndrome. Arch Neuro Psychiatr 1940, 44:841-847.
3. Brockmann K. The expanding phenotype of GLUT1-deficiency syndrome. Brain Dev 2009, 31:545-552.
4. Bruno M.K., Hallett M., Gwinn-Hardy K., Sorensen B., Considine E., Tucker S., et al. Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria. Neurology 2004, 63:2280-2287.
5. Bruno M.K., Lee H.Y., Auburger G.W., Friedman A., Nielsen J.E., Lang A.E., et al. Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia. Neurology 2007, 68:1782-1789.
6. Chen W.J., Lin Y., Xiong Z.Q., Wei W., Ni W., Tan G.H., et al. Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia. Nat Genet 2011, 43:1252-1255.
7. Cloarec R., Bruneau N., Rudolf G., Massacrier A., Salmi M., Bataillard M., et al. PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine. Neurology 2012, 79:2097-2103.
8. Gardiner A.R., Bhatia K.P., Stamelou M., Dale R.C., Kurian M.A., Schneider S.A., et al. PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. Neurology 2012, 79:2115-2121.
9. Guerrini R., Mink J.W. Paroxysmal disorders associated with PRRT2 mutations shake up expectations on ion channel genes. Neurology 2012, 79:2086-2088.
10. Marini C., Conti V., Mei D., Battaglia D., Lettori D., Losito E., et al. PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine. Neurology 2012, 79:2109-2114.
11. Meneret A., Grabli D., Depienne C., Gaudebout C., Picard F., Durr A., et al. PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population. Neurology 2012, 79:170-174.
12. Suls A., Dedeken P., Goffin K., Van Esch H., Dupont P., Cassiman D., et al. Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1. Brain 2008, 131:1831-1844.
13. van Vliet R., Breedveld G., de Rijk-van Andel J., Brilstra E., Verbeek N., Verschuuren-Bemelmans C., et al. PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions. Neurology 2012, 79:777-784.
14. Verrotti A., D'Egidio C., Agostinelli S., Gobbi G. Glut1 deficiency: when to suspect and how to diagnose?. Eur J Paediatr Neurol 2012, 16:3-9.
15. Wang J.L., Cao L., Li X.H., Hu Z.M., Li J.D., Zhang J.G., et al. Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias. Brain 2011, 134:3493-3501.
16. Weber Y.G., Storch A., Wuttke T.V., Brockmann K., Kempfle J., Maljevic S., et al. GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak. JClin Invest 2008, 118:2157-2168.
17. Blakeley J., Jankovic J. Secondary paroxysmal dyskinesias. Mov Disord 2002, 17:726-734.
18. Hur Y.J., Hwang T. Secondary paroxysmal dyskinesia associated with 2009 H1N1 infection. Korean J Pediatr 2013, 56:42-44.
19. Mirsattari S.M., Berry M.E., Holden J.K., Ni W., Nath A., Power C. Paroxysmal dyskinesias in patients with HIV infection. Neurology 1999, 52:109-114.
20. Baik J.S., Han S.W., Park J.H., Lee M.S. Psychogenic paroxysmal dyskinesia: the role of placebo in the diagnosis and management. Mov Disord 2009, 24:1244-1245.
21. Fahn S., Williams D.T. Psychogenic dystonia. Adv Neurol 1988, 50:431-455.
22. Bressman S.B., Fahn S., Burke R.E. Paroxysmal non-kinesigenic dystonia. Adv Neurol 1988, 50:403-413.
23. Demirkiran M., Jankovic J. Paroxysmal dyskinesias: clinical features and classification. Ann Neurol 1995, 38:571-579.
24. Vidailhet M., Bourdain F., Nuss P., Trocello J. Paroxysmal psychogenic movement disorders. Psychogenic movement disorders 2006, 76-81. Lippincott Williams & Wilkins, Philadelphia. S. Fahn, M. Hallet (Eds.).
25. Canavese C., Ciano C., Zibordi F., Zorzi G., Cavallera V., Nardocci N. Phenomenology of psychogenic movement disorders in children. Mov Disord 2012, 27:1153-1157.
26. Fahn S. Psychogenic movement disorders. Movement disorders 1994, 359-372. Butterworth-Heineman, Oxford. 3rd ed. C.D. Marsden, S. Fahn (Eds.).
27. Factor S.A., Podskalny G.D., Molho E.S. Psychogenic movement disorders: frequency, clinical profile, and characteristics. JNeurol Neurosurg Psychiatr 1995, 59:406-412.
28. Ranawaya R., Riley D., Lang A. Psychogenic dyskinesias in patients with organic movement disorders. Mov Disord 1990, 5:127-133.
29. Stone J., Carson A., Duncan R., Roberts R., Coleman R., Warlow C., et al. Which neurological diseases are most likely to be associated with "symptoms unexplained by organic disease". JNeurol 2012, 259:33-38.
30. Houser M.K., Soland V.L., Bhatia K.P., Quinn N.P., Marsden C.D. Paroxysmal kinesigenic choreoathetosis: a report of 26 patients. JNeurol 1999, 246:120-126.
31. Williams D.T., Ford B., Fahn S. Phenomenology and psychopathology related to psychogenic movement disorders. Adv Neurol 1995, 65:231-257.
32. Ibrahim N.M., Martino D., van de Warrenburg B.P., Quinn N.P., Bhatia K.P., Brown R.J., et al. The prognosis of fixed dystonia: a follow-up study. Parkinsonism Relat Disord 2009, 15:592-597.
33. Thomas M., Vuong K.D., Jankovic J. Long-term prognosis of patients with psychogenic movement disorders. Parkinsonism Relat Disord 2006, 12:382-387.