Autor(es): Sobue G,Senda Y,Matsuoka Y,Sobue I

Resumo: Four patients had idiopathic acute polyradiculoneuritis (Guillain-Barré syndrome) with sensory ataxia as the most prominent symptom. Sensory ataxia remained as a residue even three to five years after onset, despite good recovery of muscle weakness in five to 14 months. Sural nerve biopsy specimens disclosed a severe loss of large myelinated fibers and a high incidence of active axonal degeneration.

Imprenta: JAMA : Archives of Neurology, v. 40, n. 2, p. 86-89, 1983

Identificador do objeto digital: 10.1001/archneur.1983.04050020048009

Descritores: Guillain-Barre Syndrome - Cytopathology ; Guillain-Barre Syndrome - Pathogenesis

Data de publicação: 1983

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