dc.creatorBruck I.
dc.creatorAntoniuk S.A.
dc.creatorHalick S.M.S.
dc.creatorSpessatto A.
dc.creatorBruyn L.R.
dc.creatorRodrigues M.
dc.creatorKoneski J.
dc.creatorFacchim D.
dc.date2001
dc.date2015-06-26T14:43:56Z
dc.date2015-11-26T14:17:33Z
dc.date2015-06-26T14:43:56Z
dc.date2015-11-26T14:17:33Z
dc.date.accessioned2018-03-28T21:18:39Z
dc.date.available2018-03-28T21:18:39Z
dc.identifier
dc.identifierArquivos De Neuro-psiquiatria. , v. 59, n. 2 B, p. 407 - 410, 2001.
dc.identifier0004282X
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0035375652&partnerID=40&md5=a66eda8c8cd6d66a51e49ec5be89b926
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/95222
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/95222
dc.identifier2-s2.0-0035375652
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1243370
dc.descriptionFrom 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.description59
dc.description2 B
dc.description407
dc.description410
dc.descriptionWielawski, I., Rett syndrome: A medical odyssey (1986) Providence J Bull, , Dec 7
dc.descriptionHagberg, 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.descriptionDiagnostic criteria for Rett syndrome (1988) Ann Neurol, 23, pp. 425-428
dc.descriptionRosemberg, S., Arita, F., Campos, C., Síndrome de Rett:Análise dos primeiros 5 casos diagnosticados no Brasil (1987) Arq Neuropsiquiatr, 45, p. 143
dc.descriptionBruck, 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.descriptionHolm, V., Rett's syndrome:A progressive developmental disability in girls (1985) Dev Behav Pediatr, 6, pp. 32-36
dc.descriptionAl-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.descriptionHagberg, B., Rett syndrome:Clinical peculiarities and biological mysteries (1995) Acta Paediatr, 84, pp. 971-976
dc.descriptionKerr, A., Stephenson, J.B.P., Rett's syndrome in the west of Scotland (1985) BMJ, 291, pp. 579-582
dc.descriptionHagberg, B., Rett syndrome: Swedish approach to analysis of prevalence and cause (1985) Brain Dev, 7, pp. 277-280
dc.descriptionHagberg, B., Rett's syndrome: Prevalence and impact on progressive severe mental retardation in girls (1985) Acta Paediatr Scand, 74, pp. 405-408
dc.descriptionIyama, C.M., (1993) In Advances in Pediatrics Rett Syndrome, pp. 217-245. , St Louis,MO: Mosby Year Book
dc.descriptionClarke, A., Rett syndrome (1996) J Med Genet, 33, pp. 693-699
dc.descriptionJan, 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.descriptionHagberg, B.A., Skjeldal, O.H., Rett variants: A suggested model for inclusion criteria (1994) Pediatr Neurol, 11, pp. 5-11
dc.descriptionSwaiman, 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.descriptionBudden, S., Rett syndrome: Habilitation and managment reviewed (1997) Eur Child Adolesc Psychiatry, (1 SUPPL.), pp. 103-107
dc.descriptionHagne, 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.descriptionNaidu, S., Murphy, M., Moser, H., Rett syndrome: Natural history in 70 cases (1986) Am J Med Genet, 24, pp. 61-72
dc.descriptionHuang, T.J., Lubicky, J.P., Hammerberg, K.W., Scoliosis in Rett syndrome (1994) Orthop Rev, 23, pp. 931-937
dc.descriptionZoghbi, 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.descriptionSirianni, 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.descriptionWan, 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.descriptionBruck, 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.descriptionTang, 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.descriptionReiss, A.L., Faruque, F., Naidu, S., Neuroanatomy of Rett syndrome: A volumetric imaging study (1993) Ann Neurol, 34, pp. 227-234
dc.descriptionKitt, C.A., Wilcox, B.J., Preliminary evidence for neurodegenerative changes in the substantia nigra of Rett syndrome (1995) Neuropediatrics, 26, pp. 114-118
dc.descriptionArmstrong, 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.languagept
dc.publisher
dc.relationArquivos de Neuro-Psiquiatria
dc.rightsaberto
dc.sourceScopus
dc.titleRett Syndrome: Retrospective And Prospective Study Of 28 Patients [síndrome De Rett: Estudo Retrospectivo E Prospectivo De 28 Pacientes]
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución