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Riley-Day syndrome. Masanao OKADA 1 1Department of Pathology, Kagawa Medical School pp.296-302
Published Date 1989/4/10
DOI https://doi.org/10.11477/mf.1431906284
  • Abstract
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 Riley and Day first reported in 1949 five cases of dysautonomia under the title "Central autonomic dysfunction with defective lacrimation". Riley-Day syndrome (familial dysautonomia) is an autosomal recessive genetic disease limited to Ashkenazi Jews.

 Clinical signs of the disease are complex dysfunctions of sensory and autonomic systems. Clinical features of Riley-Day syndrome are Jewish, sensory impairment of taste, absence of overflow tears, postural hypotension, no flare response to intradermal histamine, absence of corneal sensation and poor feeding.


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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