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Amyotrophic lateral sclerosis in Brazil: Case series and review of the Brazilian literature.
Prado, Laura de Godoy Rousseff; Bicalho, Isabella Carolina Santos; Vidigal-Lopes, Mauro; Ferreira, Carla Juliana Araújo; Mageste Barbosa, Luiz Sérgio; Gomez, Rodrigo Santiago; De Souza, Leonardo Cruz; Teixeira, Antônio Lúcio.
Afiliação
  • Prado Lde G; a Postgraduate Program of Neuroscience, Federal University of Minas Gerais (UFMG) , Belo Horizonte , MG .
  • Bicalho IC; b Neuromuscular Disease Centre, Department of Neurology , University Hospital , Belo Horizonte , MG , and.
  • Vidigal-Lopes M; a Postgraduate Program of Neuroscience, Federal University of Minas Gerais (UFMG) , Belo Horizonte , MG .
  • Ferreira CJ; b Neuromuscular Disease Centre, Department of Neurology , University Hospital , Belo Horizonte , MG , and.
  • Mageste Barbosa LS; c Pneumology Department , Júlia Kubitschek Hospital, FHEMIG , Belo Horizonte , MG , Brazil.
  • Gomez RS; b Neuromuscular Disease Centre, Department of Neurology , University Hospital , Belo Horizonte , MG , and.
  • De Souza LC; b Neuromuscular Disease Centre, Department of Neurology , University Hospital , Belo Horizonte , MG , and.
  • Teixeira AL; b Neuromuscular Disease Centre, Department of Neurology , University Hospital , Belo Horizonte , MG , and.
Article em En | MEDLINE | ID: mdl-26854959
ABSTRACT
Our objective was to systematically analyse the first series of cases of amyotrophic lateral sclerosis (ALS) in Minas Gerais and to review the Brazilian literature about clinical studies in ALS. This was a cross-sectional and descriptive study of a consecutive series of patients with probable or defined sporadic ALS according to the Awaji criteria, followed at two referral centres of Belo Horizonte (South-east Brazil). Patients underwent full clinical assessment. Comparisons of patient subgroups according to disease duration and initial presentation were performed. A systematic review was performed about Brazilian clinical studies in ALS. Results showed that of the 61 enrolled patients the male/female ratio was 1.61. The mean age at onset of symptoms was 54.9 years (SD ± 11.4). Mean age at diagnosis was 56.3 years (SD ± 11.1). Regarding the initial form of presentation, 43 cases (70.5%) were spinal, 12 cases (19.7%) were generalized and six cases (9.8%) were bulbar. Eight studies were found in the systematic review. In conclusion, the profile of our sample was similar to other national and international series, except for fewer cases of bulbar ALS in our series. There are few clinical studies of ALS in Brazil. The national data of prevalence and incidence are still uncertain.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Idioma: En Ano de publicação: 2016 Tipo de documento: Article