Maladie d'Unverricht-Lündborg : Étude clinique et électrophysiologique de 19 familles maghrébines Unvem'cht-Lündborg disease: clinical and electro-physiological aspects in 19 North African families

Revue Neurologique

Volumn 154, Issue 6-7, 1998, Pages 503-507

  Gouider, R ^a,b,c   Ibrahim, S ^a,b,c   Fredji, M ^a,b,c   Gargouri, A ^a,b,c   Saidi H ^a,b,c   Ouezzani, R ^a,b,c   Malafosse, A ^a,b,c   Yahiaoui, M ^a,b,c   Grid, D ^a,b,c   Mrabet, A ^a,b,c  

^a CHARLES NICOLLE HOSPITAL   (Tunisia)

^b Hôpital Mustapha   (Morocco)

^c IBN SINA HOSPITAL   (Morocco)

Author keywords

[No Author keywords available]

Indexed keywords

CLONAZEPAM; PHENOBARBITAL; VALPROIC ACID;

ADULT; ALGERIA; ANTICONVULSANT THERAPY; ARTICLE; ATAXIA; CHROMOSOME 21Q; CLINICAL ARTICLE; ELECTROENCEPHALOGRAM; FEMALE; GENETIC LINKAGE; HUMAN; INCIDENCE; MALE; MOROCCO; MYOCLONUS; PHOTOSENSITIVITY; SEIZURE; SYNDROME; TUNISIA; ADOLESCENT; BIOPSY; CEREBELLUM; CLINICAL TRIAL; ELECTROENCEPHALOGRAPHY; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; GENETICS; MIDDLE AGED; MULTICENTER STUDY; MYOCLONUS EPILEPSY; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; RETROSPECTIVE STUDY; SKELETAL MUSCLE;

ADOLESCENT; ADULT; AGE OF ONSET; ALGERIA; BIOPSY; CEREBELLUM; ELECTROENCEPHALOGRAPHY; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; EPILEPSIES, MYOCLONIC; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MOROCCO; MUSCLE, SKELETAL; PEDIGREE; RETROSPECTIVE STUDIES; TUNISIA;

EID: 0031858079     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)

1. ACHARYA J.N., SATISHCHANDRA P., SHANKAR S.K. (1995). Familial progressive myoclonus epilepsy: clinical and electro-physiologic observations. Epilepsia, 36: 429-434.
2. BATTAGUA D., GENTON P., REMY C., BUREAU M., DRAVET C. (1995). Effet antimyoclonique du piracetam dans l'épilepsie myoclonique progressive de type Unverricht-Lundborg: observation clinique et vidéo. Epilepsies, 7:387-391.
3. BAULAC M., UBAUGE P., PELUSSIER J.-F. (1997). Epilepsie et détérioration intellectuelle chez une adolescente de 15 ans. Revue Neurol (Paris), 163: 72,793-801.
4. COCHIUS J.L., FiGLEwicz D.A., KALVIAINEN R., NOUSIAINEN U., FARRELL K., PATRY G., SODERFELT B., FRYDMANN M., LERMAN P., ANDERMANN F., ANDERMANN E., ROULEAU G.A. (1993). Unverricht-Lundborg disease: absence of nonallelic genetic heterogeneity. Ann Neural 34:739-741.
5. COCHIUS J., CARPENTER S., ANDERMANN E., ROULEAU G., NOUSIAINEN U., KALWJNEN R., FARRELL K., ANDERMANN F. (1994). Sweat gland vacuoles in Unverricht-Lundborg disease: a clue to diagnosis? Neurology, 44:2372-2375.
6. ELDRIDGE R., IVANAINEN M., STERN R., KOERBERT. et WILDER B.J. (1983). Baltic myoclonus epilepsy: hereditary disorder of childhood made worse by phenytoin. Lancet, 838-42.
7. FRANCESCHETTI S., ANTOZZI C., BINELJJ S., CARRARA F., NARDOCCI N., ZEVIANI M., AVANZINI G. (1993). Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases. Acta Neurol Scand, 87: 219-223.
8. GENTON P., MICHELUCCI R., TASSINARI C.A., ROGER J. (1990). The Ramsay-Hunt syndrome revisited: Mediterranean myoclonus versus mitochondrial encephalo-myopathy with ragged-red fibres and Baltic myoclonus. Acta Neurol Scand 81: 8-15.
9. KOSKINIEMI M., DONER M., MAJURI H., HALTIA M., and NORIA R. (1974). Progressive myoclonus epilepsy. A clinical and histopathological study. Acta Neurol Scand, 50: 307-332.
10. KOSKINIEMI M.L. (1986). Baltic Myoclonus In Fahn S., Marsden C.D., Van Woert M. (eds.), Advances in Neurology, Vol. 43, 57-64. Raven Press, New York.
11. LABAUGEP.,OUAZZANlR., MRABET A., GRID J., GENTON P., DRAVETC.H., CHKIU T., BECK C., BURESI C., BALDY-MOUUNIER M., MALAFOSSE A. (1997). Allelic heterogeneity of mediterranean myoclonus and the cystatin B. Ann Neurol, 41: 686-689.
12. LAFRENIERE R.G., ROCHEFORT D.L., CHRETIEN N., ROMMENS Ü.M., CocHiusJ.L, KALVIAINEN R., NOUISIANEN U., PATRY G., FARREL K., SODERFEDT B., FEDERICO A., HALE B.R. COSSIO O.H., SORENSEN T., POUUOT M.A., KMIEC T., ULDALL P., JANSZKY J., PRANZATELU M.R., ANDERMANN E. et ROULEAU G.A. (1997). Unstable insertion in thé 5' flanking region of the cystatin B gene in the most commun mutation in the progressive myoclonus type 1 E.P.M.1. Nature Genetics, 15:: 298-302.
13. .LEHESJOKI A.E., KOSKINIEMI M., SISTONEN P., MIAO J., HASTBACKA J., NORIO R., DE LA CHAPELLE A. (1991). Localization of a gene for progressive myoclonus epilepsy to chromosome 21 q22. ProcNatl Acad Sei USA 88: 3696-3699.
14. LEHESJOKI A.E., ELDRIDGE R., ELDRIDGE J., WILDER B.J., DE LA CHAPELLE, (1993). Progressive myoclonus epilepsy of Unverricht-Lundborg type: a clinical and molecular genetic study of a family from the United States with four affected sibs. Neurology 43: 2384-2386.
15. LEHESJOKI A.E., TASSINARI C.A., AVANZINI G., MICHELUCCI R., FRANCESCHETTI S., ANTONELU A., RUBBOU G., DE LA CHAPELLE A. (1994). PME of Unverricht-Lundborg type in the Mediterranean region: linkage and linkage disequilibrium confim the assignment to the EPM1 locus. Hum Genet 93: 668-674.
16. MALAFOSSE A., LEHESJOKI A.E., GENTON P LABAUGE P., DURAND G., TASSINARI C.A., DRAVETC., MICHELUCCI R., DE LA CHAPELLE A. (1992). Identical genetic locus for Baltic and Mediterranean myoclonus. Lancet 339:1080-1081.
17. MARSEILLE CONSENSUS GROUP. (1990). Classification of progressive myoclonus epilepsies and related disorders. Ann Neurol, 28 : 113-116.
18. PENNACHIO L.A., LEHESJOKI A.E., STONE N.E., WILLOUR V.L., VIRTANEVA K., MIAO J., D'AMATO E., RAMIREZ L, FAHAM M., KOSKINIEMI M., WARRINGTON J.A., NORIO R., DE LA CHAPELLE A., Cox D.R., MYERS R.M. (1996). Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EMP1). Science, 271:1731-1733.