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Refsum's disease may mimic familial Guillain Barre syndrome.
Verny, Christophe; Prundean, Adriana; Nicolas, Guillaume; Pautot, Vivien; Maugin, Dominique; Levade, Thierry; Bonneau, Dominique; Dubas, Frederic.
Afiliação
  • Verny C; Centre national de référence des maladies neurogénétiques et cytopathies mitochondriales de l'adulte, Centre Hospitalier Universitaire, Angers, France. chverny@chu-angers.fr
Neuromuscul Disord ; 16(11): 805-8, 2006 Nov.
Article em En | MEDLINE | ID: mdl-16934464
Refsum's disease is a rare autosomal recessive disorder with clinical features including retinitis pigmentosa, anosmia, deafness, chronic sensory-motor neuropathy, ataxia and the accumulation of phytanic acid in blood plasma and body tissues. We report the occurrence of Refsum's disease in two sisters, both presenting with acute demyelinating polyneuropathy mimicking the familial Guillain Barre syndrome. Thus, when GBS is suspected, particularly in cases of familial recurrence as well as in atypical cases of acute polyneuropathy, the diagnosis of Refsum's disease should be considered, looking for other features of the disease and, if appropriate, testing plasma phytanic acid levels.
Assuntos
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Bases de dados: MEDLINE Assunto principal: Doença de Refsum / Síndrome de Guillain-Barré Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: En Revista: Neuromuscul Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2006 Tipo de documento: Article País de afiliação: França
Buscar no Google
Bases de dados: MEDLINE Assunto principal: Doença de Refsum / Síndrome de Guillain-Barré Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: En Revista: Neuromuscul Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2006 Tipo de documento: Article País de afiliação: França