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Finger drop sign as a new variant of acute motor axonal neuropathy.
Yoon, Byeol-A; Ha, Dong-Ho; Park, Hwan Tae; Kusunoki, Susumu; Kuwahara, Motoi; Lee, Jong Hwa; Bae, Jong Seok; Kim, Jong Kuk.
  • Yoon BA; Department of Neurology, Dong-A University College of Medicine, Busan, Republic of Korea.
  • Ha DH; Department of Peripheral Neuropathy Research Center, Dong-A University College of Medicine, Busan, Republic of Korea.
  • Park HT; Department of Radiology, Dong-A University College of Medicine, Busan, Republic of Korea.
  • Kusunoki S; Department of Peripheral Neuropathy Research Center, Dong-A University College of Medicine, Busan, Republic of Korea.
  • Kuwahara M; Department of Molecular Neuroscience, Dong-A University College of Medicine, Busan, Republic of Korea.
  • Lee JH; Department of Neurology, Kindai University College of Medicine, Osaka, Japan.
  • Bae JS; Department of Neurology, Kindai University College of Medicine, Osaka, Japan.
  • Kim JK; Department of Physical Medicine and Rehabilitation, Dong-A University College of Medicine, Busan, Republic of Korea.
Muscle Nerve ; 63(3): 336-343, 2021 03.
Article en En | MEDLINE | ID: mdl-33217007
ABSTRACT
We propose the finger drop sign as a new clinical variant of acute motor axonal neuropathy (AMAN) defined by immunological and radiological evidence. We identified eight consecutive patients who had AMAN. All of them developed prominent involvement of the finger extensors. We performed magnetic resonance imaging (MRI) of the extremity muscles and serological assays for antiganglioside antibodies and Campylobacter jejuni. Patients with AMAN showed characteristic and a markedly sustained weakness of the finger extensors with a distinctive pattern of the finger drop sign. Limb MRI revealed unevenly distributed abnormal signals in the muscles mainly innervated by the posterior interosseous nerve. All tested patients showed positivity for immunoglobulin G antibody against ganglioside complex of GM1 and phosphatidic acid. A pathophysiological understanding of this unique syndrome can provide further insight into antiganglioside-antibody-mediated axonal injury in Guillain-Barré syndrome.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ácidos Fosfatidicos / Autoanticuerpos / Axones / Debilidad Muscular / Síndrome de Guillain-Barré / Dedos / Gangliósido G(M1) / Conducción Nerviosa Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ácidos Fosfatidicos / Autoanticuerpos / Axones / Debilidad Muscular / Síndrome de Guillain-Barré / Dedos / Gangliósido G(M1) / Conducción Nerviosa Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2021 Tipo del documento: Article