Idiopathic dystonia clinical, profile of 76 brazilian patients

Detalhes bibliográficos
Autor(a) principal: Andrade, Luiz A. F. [UNIFESP]
Data de Publicação: 1992
Outros Autores: Ferraz, Henrique B. [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0004-282X1992000400003
http://repositorio.unifesp.br/handle/11600/306
Resumo: Dystonia may be classified by age of onset (childhood, adolescence, adult onset), body distribution of the abnormal movements (focal, segmental, unilateral, multifocal and generalized) and etiology (idiopathic and symptomatic). We studied 76 patients with idiopathic dystonia among 122; cases of dystonic syndrome (62.3% of the total). There were 48 female and 28 male patients. Adult-onset focal dystonia was the most frequent feature (37 patients). The onset of generalized dystonia was more frequently seen under the age of 20, whereas focal and segmental dystonia usually started over this age. Postural tremor of the hands was observed in 19.7% of the patients. Spasmodic torticollis was the most prevalent form of dystonia overall. Except for writer's cramp, which occurred more frequently in males, and generalized dystonia, which was equally divided between sexes, all other forms were more frequent in females. Our data suggest that differences in racial origin, social and economical status and environmental factors do not account for a different manifestation in dystonia pattern.
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spelling Idiopathic dystonia clinical, profile of 76 brazilian patientsDistonia idiopática: perfil clínico de 76 pacientes brasileirosdystoniadystonia musculorum deformansidiopathic dystoniadistoniadystonia musculorum deformansdistonia idiopáticaDystonia may be classified by age of onset (childhood, adolescence, adult onset), body distribution of the abnormal movements (focal, segmental, unilateral, multifocal and generalized) and etiology (idiopathic and symptomatic). We studied 76 patients with idiopathic dystonia among 122; cases of dystonic syndrome (62.3% of the total). There were 48 female and 28 male patients. Adult-onset focal dystonia was the most frequent feature (37 patients). The onset of generalized dystonia was more frequently seen under the age of 20, whereas focal and segmental dystonia usually started over this age. Postural tremor of the hands was observed in 19.7% of the patients. Spasmodic torticollis was the most prevalent form of dystonia overall. Except for writer's cramp, which occurred more frequently in males, and generalized dystonia, which was equally divided between sexes, all other forms were more frequent in females. Our data suggest that differences in racial origin, social and economical status and environmental factors do not account for a different manifestation in dystonia pattern.A distonia pode ser classificada de acordo com a idade de início (infância, adolescência e idade adulta), distribuição corporal dos movimentos anormais (focal, segmentar, unilateral, multifocal e generalizada) e etiologia (idiopática e sintomática). Dentre 122 pacientes com o diagnóstico de síndrome distônica, estudamos 76 com quadros idiopáticos (62,3% do total). Havia 48 pacientes do sexo feminino e 28 do sexo masculino. O quadro mais frequentemente observado foi a da distonia focal iniciada na idade adulta. (37 pacientes). Havia 6 pacientes com distonia generalizada e o início desse quadro foi mais frequento abaixo dos 20 anos de idade. Quadros focais e segmentares predominaram e foram mais comumentemente iniciados na idade adulta. Tremor postural das mãos foi observado em 15 pacientes (19,7%). De todas as formas de distonia, o torcicolo espasmódico foi a que prevaleceu. Com a exceção da cãimbra do escrivão (com mais homens que mulheres acometidas) e da distonia generalizada (a mesma proporção entre os sexos), o sexo feminino predominou sobre o masculino. Nossos dados são semelhantes aos de outras séries que estudaram o quadro clínico da distonia idiopática. Assim, diferenças raciais, ambientais e sócio-econômicas não parecem ser determinantes: no padrão de manifestação da distonia idiopática.Escola Paulista de Medicina Department of Neurology and NeurosurgeryUNIFESP, EPM, Department of Neurology and NeurosurgerySciELOConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Academia Brasileira de Neurologia - ABNEUROUniversidade Federal de São Paulo (UNIFESP)Andrade, Luiz A. F. [UNIFESP]Ferraz, Henrique B. [UNIFESP]2015-06-14T13:24:23Z2015-06-14T13:24:23Z1992-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion426-432application/pdfhttp://dx.doi.org/10.1590/S0004-282X1992000400003Arquivos de Neuro-Psiquiatria. Academia Brasileira de Neurologia - ABNEURO, v. 50, n. 4, p. 426-432, 1992.10.1590/S0004-282X1992000400003S0004-282X1992000400003.pdf0004-282XS0004-282X1992000400003http://repositorio.unifesp.br/handle/11600/306engArquivos de Neuro-Psiquiatriainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-28T11:02:04Zoai:repositorio.unifesp.br/:11600/306Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-28T11:02:04Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Idiopathic dystonia clinical, profile of 76 brazilian patients
Distonia idiopática: perfil clínico de 76 pacientes brasileiros
title Idiopathic dystonia clinical, profile of 76 brazilian patients
spellingShingle Idiopathic dystonia clinical, profile of 76 brazilian patients
Andrade, Luiz A. F. [UNIFESP]
dystonia
dystonia musculorum deformans
idiopathic dystonia
distonia
dystonia musculorum deformans
distonia idiopática
title_short Idiopathic dystonia clinical, profile of 76 brazilian patients
title_full Idiopathic dystonia clinical, profile of 76 brazilian patients
title_fullStr Idiopathic dystonia clinical, profile of 76 brazilian patients
title_full_unstemmed Idiopathic dystonia clinical, profile of 76 brazilian patients
title_sort Idiopathic dystonia clinical, profile of 76 brazilian patients
author Andrade, Luiz A. F. [UNIFESP]
author_facet Andrade, Luiz A. F. [UNIFESP]
Ferraz, Henrique B. [UNIFESP]
author_role author
author2 Ferraz, Henrique B. [UNIFESP]
author2_role author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Andrade, Luiz A. F. [UNIFESP]
Ferraz, Henrique B. [UNIFESP]
dc.subject.por.fl_str_mv dystonia
dystonia musculorum deformans
idiopathic dystonia
distonia
dystonia musculorum deformans
distonia idiopática
topic dystonia
dystonia musculorum deformans
idiopathic dystonia
distonia
dystonia musculorum deformans
distonia idiopática
description Dystonia may be classified by age of onset (childhood, adolescence, adult onset), body distribution of the abnormal movements (focal, segmental, unilateral, multifocal and generalized) and etiology (idiopathic and symptomatic). We studied 76 patients with idiopathic dystonia among 122; cases of dystonic syndrome (62.3% of the total). There were 48 female and 28 male patients. Adult-onset focal dystonia was the most frequent feature (37 patients). The onset of generalized dystonia was more frequently seen under the age of 20, whereas focal and segmental dystonia usually started over this age. Postural tremor of the hands was observed in 19.7% of the patients. Spasmodic torticollis was the most prevalent form of dystonia overall. Except for writer's cramp, which occurred more frequently in males, and generalized dystonia, which was equally divided between sexes, all other forms were more frequent in females. Our data suggest that differences in racial origin, social and economical status and environmental factors do not account for a different manifestation in dystonia pattern.
publishDate 1992
dc.date.none.fl_str_mv 1992-12-01
2015-06-14T13:24:23Z
2015-06-14T13:24:23Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0004-282X1992000400003
Arquivos de Neuro-Psiquiatria. Academia Brasileira de Neurologia - ABNEURO, v. 50, n. 4, p. 426-432, 1992.
10.1590/S0004-282X1992000400003
S0004-282X1992000400003.pdf
0004-282X
S0004-282X1992000400003
http://repositorio.unifesp.br/handle/11600/306
url http://dx.doi.org/10.1590/S0004-282X1992000400003
http://repositorio.unifesp.br/handle/11600/306
identifier_str_mv Arquivos de Neuro-Psiquiatria. Academia Brasileira de Neurologia - ABNEURO, v. 50, n. 4, p. 426-432, 1992.
10.1590/S0004-282X1992000400003
S0004-282X1992000400003.pdf
0004-282X
S0004-282X1992000400003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Arquivos de Neuro-Psiquiatria
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 426-432
application/pdf
dc.publisher.none.fl_str_mv Academia Brasileira de Neurologia - ABNEURO
publisher.none.fl_str_mv Academia Brasileira de Neurologia - ABNEURO
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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