Idiopathic dystonia clinical, profile of 76 brazilian patients
Autor(a) principal: | |
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Data de Publicação: | 1992 |
Outros Autores: | |
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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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 |
_version_ |
1814268370161238016 |