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Japanese

An Autopsy Case of Hallervorden-Spatz Disease: Clinicopathological and Biochemical Study Sachio Takashima 1 , Yashushi Iwata 1 , Kenzo Tanaka 1 , Toru Kurokawa 2 , Kenzo Takeshita 2 , Tokuro Nagayama 2 , Yasuo Ito 3 , Haruo Uzawa 3 1First Dept. of Pathology, Faculty of Med., Kyushu Univ. 2Dept. of Pediatrics, Faculty of Med., Kyushu Univ. 3Second Dept. of Internal Medicine, Faculty of Med., Kyushu Univ. pp.249-259
Published Date 1969/6/25
DOI https://doi.org/10.11477/mf.1431906443
  • Abstract
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An autopsy case of 13-year-old boy with Hallervorden-Spatz disease was reported. His family history revealed the consanguineous marriage of his parents and retinal degeneration of his younger sister. Night blindness and febrile convulsions were noticed in the early childhood. He suffered from indistinct speech and squint since 7 years of age. When he was 9 years old, he became awkward in his writing and walking and developed athetoid movements of the right upper extremity.


Copyright © 1969, 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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