A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.
Autor(es): Barbieri F.; Santangelo R.; Crisci C.; Ragno M.; Perretti A.; Santoro L.
Resumo: The appearance of Guillain-Barré syndrome in a 9-year-old girl led to the detection of a hereditary neuropathy in her family. This neuropathy showed clinical and electrophysiological characteristics of Charcot-Marie-Tooth disease. Only nerve biopsy performed in a sister of the proband allowed diagnosis of tomaculous neuropathy which presented unusual clinical, electrophysiological and bioptic aspects.
Imprenta: Clinical Neurology and Neurosurgery, v. 92, n. 3, p. 289-294, 1990
Identificador do objeto digital: 10.1016/0303-8467(90)90037-6
Descritores: Guillain-Barre Syndrome - Cell ; Guillain-Barre Syndrome - Cytopathology ; Guillain-Barre Syndrome - Pathogenesis
Data de publicação: 1990
