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Acute pandysautonomia. Toru OKAJIMA 1 1Department of Medicine, Medical College of Oita pp.269-281
Published Date 1989/4/10
DOI https://doi.org/10.11477/mf.1431906282
  • Abstract
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 Acute dysautonomia has been reported in various terms. Acute pandysautonomia (APD) was originally described as a 'pure' entity with exclusive involvement of the autonomic nerves (Young et al., 1969), but in the subsequent reports, not a few cases with paresthesia or slight sensory deficit were seen. Acute dysautonomia with severe sensory or sensorimotor disturbances were also reported. On the autonomic disorders, there were no differences among these conditions, so I made a following classification, and clinical features were analyzed in 51 cases reported.

 1) acute idiopathic pandysautonomia (AIPD)

 2) acute post- or parainfectious pandysautonomia (APPD)

 3) acute autonomic and sensory neuropathy (AASN)

 4) acute autonomic and sensorimotor neuropathy (AASM)

 5) acute cholinergic neuropathy (ACN)

 6) unclassified


Copyright © 1989, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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