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A case of Crouzon's disease. Norio Yuge 1 , Toshi Shimazaki 2 1Kyoto Prefectural University of Medicine. Department of Ophthalmology. 2Kyoto Prefectural University of Medicine. Department of Radiology. pp.1251-1254
Published Date 1960/8/15
DOI https://doi.org/10.11477/mf.1410207013
  • Abstract
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A case of Crouzon's disease (Dysostose cranio-faciale hereditaire) is reported in this paper. This female patient, aged 12, with marked exophthalmos has a cousin whose face is similar to hers. Examination showed marked exophthalmos (right 24mm and left 26mm by Hertel's exophthalmometer), exotropia, disturbed motility of the eye ball expecially the left eye and prognathism. Vision was : R.E. 0.7 : L.E. not clear. The skull X-ray revealed impressio digitale, hypoplasia of maxillary bone and pseudoprognathism.


Copyright © 1960, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1308 印刷版ISSN 0370-5579 医学書院

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