| dc.creator | Bruck I. | |
| dc.creator | Antoniuk S.A. | |
| dc.creator | Halick S.M.S. | |
| dc.creator | Spessatto A. | |
| dc.creator | Bruyn L.R. | |
| dc.creator | Rodrigues M. | |
| dc.creator | Koneski J. | |
| dc.creator | Facchim D. | |
| dc.date | 2001 | |
| dc.date | 2015-06-26T14:43:56Z | |
| dc.date | 2015-11-26T14:17:33Z | |
| dc.date | 2015-06-26T14:43:56Z | |
| dc.date | 2015-11-26T14:17:33Z | |
| dc.date.accessioned | 2018-03-28T21:18:39Z | |
| dc.date.available | 2018-03-28T21:18:39Z | |
| dc.identifier | | |
| dc.identifier | Arquivos De Neuro-psiquiatria. , v. 59, n. 2 B, p. 407 - 410, 2001. | |
| dc.identifier | 0004282X | |
| dc.identifier | | |
| dc.identifier | http://www.scopus.com/inward/record.url?eid=2-s2.0-0035375652&partnerID=40&md5=a66eda8c8cd6d66a51e49ec5be89b926 | |
| dc.identifier | http://www.repositorio.unicamp.br/handle/REPOSIP/95222 | |
| dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/95222 | |
| dc.identifier | 2-s2.0-0035375652 | |
| dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1243370 | |
| dc.description | From November 1982 to May 1999, 28 children with Rett syndrome were followed-up for a medium period of 6 years and 2 months. Regression of developmental milestones started at the age between 5 and 20 months. Nineteen cases of typical Rett syndrome had uneventful pre and perinatal periods, loss of previously acquired purposeful hand skills, mental and motor regression and developed hand stereotypies; sixteen had head growth deceleration and 12 gait apraxia. Nine patients were atypical cases, 2 formes frustres, 2 congenital, 3 with early seizure onset, 1 preserved speech and 1 male. Epilepsy was present in 21 patients, predominantly partial seizures and the drug of choise was carbamazepine (15 patients). In the initial evaluation most patients were distributed on Stages II and III and on follow-up on Stages III and IV. Three children died. | |
| dc.description | 59 | |
| dc.description | 2 B | |
| dc.description | 407 | |
| dc.description | 410 | |
| dc.description | Wielawski, I., Rett syndrome: A medical odyssey (1986) Providence J Bull, , Dec 7 | |
| dc.description | Hagberg, B., Aicardi, J., Dias, K., A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases (1983) Ann Neurol, 14, pp. 471-479 | |
| dc.description | Diagnostic criteria for Rett syndrome (1988) Ann Neurol, 23, pp. 425-428 | |
| dc.description | Rosemberg, S., Arita, F., Campos, C., Síndrome de Rett:Análise dos primeiros 5 casos diagnosticados no Brasil (1987) Arq Neuropsiquiatr, 45, p. 143 | |
| dc.description | Bruck, I., Antoniuk, S.A., De Paola, D., Araki, T.Y., Flenik, L.T., Síndrome de Rett:Relato de 7 casos (1990) Arq Neuropsiquiatr, 48, pp. 489-492 | |
| dc.description | Holm, V., Rett's syndrome:A progressive developmental disability in girls (1985) Dev Behav Pediatr, 6, pp. 32-36 | |
| dc.description | Al-Mateen, M., Philipart, M., Shields, D., Rett syndrome: A commonly overlooked progressive encephalopathy in girls (1986) Am J Dis Child, 140, pp. 761-765 | |
| dc.description | Hagberg, B., Rett syndrome:Clinical peculiarities and biological mysteries (1995) Acta Paediatr, 84, pp. 971-976 | |
| dc.description | Kerr, A., Stephenson, J.B.P., Rett's syndrome in the west of Scotland (1985) BMJ, 291, pp. 579-582 | |
| dc.description | Hagberg, B., Rett syndrome: Swedish approach to analysis of prevalence and cause (1985) Brain Dev, 7, pp. 277-280 | |
| dc.description | Hagberg, B., Rett's syndrome: Prevalence and impact on progressive severe mental retardation in girls (1985) Acta Paediatr Scand, 74, pp. 405-408 | |
| dc.description | Iyama, C.M., (1993) In Advances in Pediatrics Rett Syndrome, pp. 217-245. , St Louis,MO: Mosby Year Book | |
| dc.description | Clarke, A., Rett syndrome (1996) J Med Genet, 33, pp. 693-699 | |
| dc.description | Jan, M.M.S., Dooley, J.M., Gordon, K.E., Male Rett syndrome variant: Aplication of diagnostic criteria (1999) Pediatr Neurol, 20, pp. 238-240 | |
| dc.description | Hagberg, B.A., Skjeldal, O.H., Rett variants: A suggested model for inclusion criteria (1994) Pediatr Neurol, 11, pp. 5-11 | |
| dc.description | Swaiman, K.F., Dyken, R.D., Rett syndrome (1999) Pediatric Neurology, Principles & Pratice. 3ed., 2, pp. 836-839. , Swaiman KF, Ashwal S, (eds) St Louis: Mosby Inc | |
| dc.description | Budden, S., Rett syndrome: Habilitation and managment reviewed (1997) Eur Child Adolesc Psychiatry, (1 SUPPL.), pp. 103-107 | |
| dc.description | Hagne, I., Witt-Engerstrom, I., Hagberg, B., EEg development in Rett syndrome: A study of 30 cases (1989) Eletroencephalogr Clin Neurophysiol, 72, pp. 1-6 | |
| dc.description | Naidu, S., Murphy, M., Moser, H., Rett syndrome: Natural history in 70 cases (1986) Am J Med Genet, 24, pp. 61-72 | |
| dc.description | Huang, T.J., Lubicky, J.P., Hammerberg, K.W., Scoliosis in Rett syndrome (1994) Orthop Rev, 23, pp. 931-937 | |
| dc.description | Zoghbi, H.Y., Percy, A.K., Schultz, R.J., Fill, C., Patterns of X chromosome inactivation in the Rett syndrome (1990) Brain Dev, 12, pp. 131-135 | |
| dc.description | Sirianni, N., Naidu, S., Pereira, J.L., Pillotto, R.F., Hoffman, E.P., Rett syndrome, confirmation of x-linked dominant inheritance, and localization of the gene to Xq28 (1998) Am J Hum Genet, 63, pp. 1552-1558 | |
| dc.description | Wan, M., Lee, S.S.J., Zhang, X., Rett syndrome and beyond: Recurrent spontaneous and familial MECP2 mutations at CpG hotspots (1999) Am J Hum Genet, 65, pp. 1520-1529 | |
| dc.description | Bruck, I., Philippart, M., Giraldi, D., Antoniuk, S., Difference in early development of presumed monozygotic twins with Rett syndrome (1991) Am J Med Genet, 39, pp. 415-417 | |
| dc.description | Tang, J., Qi, Y., Bao, X.H., Wu, X.R., Mutational analysis of mitochondrial DNA of children with Rett syndrome (1997) Pediatr Neurol, 17, pp. 327-330 | |
| dc.description | Reiss, A.L., Faruque, F., Naidu, S., Neuroanatomy of Rett syndrome: A volumetric imaging study (1993) Ann Neurol, 34, pp. 227-234 | |
| dc.description | Kitt, C.A., Wilcox, B.J., Preliminary evidence for neurodegenerative changes in the substantia nigra of Rett syndrome (1995) Neuropediatrics, 26, pp. 114-118 | |
| dc.description | Armstrong, D., Dunn, J.K., Antalffy, B., Trivedi, R., Seletive dendritic alterations in the cortex of Rett syndrome (1995) J Neuropathol Exp Neurol, 54, pp. 195-201 | |
| dc.language | pt | |
| dc.publisher | | |
| dc.relation | Arquivos de Neuro-Psiquiatria | |
| dc.rights | aberto | |
| dc.source | Scopus | |
| dc.title | Rett Syndrome: Retrospective And Prospective Study Of 28 Patients [síndrome De Rett: Estudo Retrospectivo E Prospectivo De 28 Pacientes] | |
| dc.type | Artículos de revistas | |