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Guillain-Barré syndrome subtypes: A clinical electrophysiological study of 100 patients.
Grapperon, A-M; Berro, M; Salort-Campana, E; Verschueren, A; Delmont, E; Attarian, S.
Afiliação
  • Grapperon AM; Referral Center for Neuromuscular Diseases and ALS, AP-HM, Timone University Hospital, 13385 Marseille, France. Electronic address: aude-marie.grapperon@ap-hm.fr.
  • Berro M; Referral Center for Neuromuscular Diseases and ALS, AP-HM, Timone University Hospital, 13385 Marseille, France.
  • Salort-Campana E; Referral Center for Neuromuscular Diseases and ALS, AP-HM, Timone University Hospital, 13385 Marseille, France.
  • Verschueren A; Referral Center for Neuromuscular Diseases and ALS, AP-HM, Timone University Hospital, 13385 Marseille, France.
  • Delmont E; Referral Center for Neuromuscular Diseases and ALS, AP-HM, Timone University Hospital, 13385 Marseille, France; CNR2M, CNRS UMR 7286, Aix-Marseille University, 13005 Marseille, France.
  • Attarian S; Referral Center for Neuromuscular Diseases and ALS, AP-HM, Timone University Hospital, 13385 Marseille, France; INSERM UMR S 910, Aix-Marseille University, 13005 Marseille, France.
Rev Neurol (Paris) ; 175(1-2): 73-80, 2019.
Article em En | MEDLINE | ID: mdl-30442448
INTRODUCTION: A retrospective analysis was performed to document the clinical and electrophysiological features of Guillain-Barré syndrome (GBS) subtypes using different diagnostic criteria. METHODS: One hundred GBS patients were included. Clinical and laboratory features were analyzed, and patients were classified according to four sets of diagnostic criteria. Electrodiagnostic criteria were also analyzed. RESULTS: A total of 69 patients met Asbury and Cornblath's criteria, 96 met Van der Meché's criteria, 99 met Wakerley's diagnostic classification and 86 met level 1 or 2 of the Brighton criteria. Rates of GBS subtypes were: 69% classic GBS; 8% Miller-Fisher syndrome; 12% paraparetic GBS; 2% pharyngeal-cervical-brachial GBS; and 9% unclassified. Those for electrodiagnostic subtypes were 52% demyelinating and 9% axonal according to Hadden's criteria vs 41% demyelinating and 41% axonal as per Rajabally's criteria. CONCLUSION: In this study of case distribution within the GBS spectrum of a retrospective cohort of French patients, the application of new diagnostic criteria enabled accurate diagnoses and classifications of the different subtypes, and also increased the recognition of axonal GBS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Guillain-Barré Tipo de estudo: Observational_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Rev Neurol (Paris) Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Guillain-Barré Tipo de estudo: Observational_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Rev Neurol (Paris) Ano de publicação: 2019 Tipo de documento: Article