Partial Epilepsy and 47,XXX Karyotype: Report of Four Cases

Pediatric Neurology

Volumn 35, Issue 1, 2006, Pages 69-74

  Roubertie, Agathe ^a   Humbertclaude, Véronique ^b   Leydet, Julie ^a   Lefort, Geneviève ^c   Echenne, Bernard ^a  

^a GUI DE CHAULIAC HOSPITAL   (France)

^b Institut Saint Pierre   (France)

^c HÔPITAL ARNAUD DE VILLENEUVE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CHILD; EPILEPSY; HUMAN; KARYOTYPE 45,X; MENTAL DEFICIENCY; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIORITY JOURNAL; SEIZURE; SEX CHROMOSOME ABERRATION; TRISOMY; X CHROMOSOME;

CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, X; EPILEPSIES, PARTIAL; FEMALE; HUMANS; INFANT; TRISOMY;

EID: 33745279595     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2006.01.003     Document Type: Article

References (14)

1. Singh R., Gardner R.J., Crossland K.M., Scheffer I.E., and Berkovic S.F. Chromosomal abnormalities and epilepsy. A review for clinicians and gene hunters. Epilepsia 43 (2002) 127-140
2. Inoue Y., Fujiwara T., Matsuda K., et al. Ring chromosome 20 and nonconvulsive status epilepticus. A new epileptic syndrome. Brain 120 (1997) 939-953
3. Ieshima A., and Takeshita K. Chromosome abnormalities and epileptic seizures. Jinrui Idengaku Zasshi 33 (1988) 49-60
4. Linden M.G., and Bender B.G. Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities. Am J Med Genet 110 (2002) 11-18
5. Haverty C.E., Lin A.E., Simpson E., Spence M.A., and Martin R.A. 47,XXX associated with malformations. Am J Med Genet 125A (2004) 108-111
6. Guichet A., Briault S., Moraine C., and Turleau C. Trisomy X. ACLF retrospective study. Ann Genet 39 (1996) 117-122
7. Bender B.G., Harmon R.J., Linden M.G., and Robinson A. Psychosocial adaptation of 39 adolescents with sex chromosome abnormalities. Pediatrics 96 (1995) 302-308
8. Harmon R.J., Bender B.G., Linden M.G., and Robinson A. Transition from adolescence to early adulthood. Adaptation and psychiatric status of women with 47,XXX. J Am Acad Child Adolesc Psychiatry 37 (1998) 286-291
9. Rovet J., Netley C., Bailey J., Keenan M., and Stewart D. Intelligence and achievement in children with extra X aneuploidy. A longitudinal perspective. Am J Med Genet 60 (1995) 356-363
10. Takei H., Asaka A., and Kurihara T. [2 cases of triplo-X with epileptic seizure]. No To Shinkei 21 (1969) 523-532
11. Sills J.A., Brown J.K., Grace E., Wood S.M., Barclay G.R., and Urbaniak S.J. XXX syndrome associated with immunoglobulin deficiency and epilepsy. J Pediatr 93 (1978) 469-471
12. Macleod S., Mallik A., Tolmie J.L., Stephenson J.B.P., O'Regan M.E., and Zuberi S. Electro-clinical phenotypes of chromosome disorders associated with epilepsy in the absence of dysmorphism. Brain Dev 27 (2005) 118-124
13. Grosso S., Farnetani M.A., Di Bartolo R.M., et al. Electroencephalographic and epileptic patterns in X chromosome anomalies. J Clin Neurophysiol 21 (2004) 249-253
14. Chiurazzi P., Hamel B.C., and Neri G. XLMR genes. Updates 2000. Eur J Med Genet 9 (2001) 71-81