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Japanese

A Case of Hurler Syndrome (Scheie Syndrome) Kiyoji Fukunaga 1 , Akihiko Tamai 1 , Takeshi Watanabe 1 , Yutaka Fujinaga 1 , Tsutomu Nishigori 1Department of Ophthalmology, Tottori Univcrsity School of Medicine pp.1405-1411
Published Date 1971/5/15
DOI https://doi.org/10.11477/mf.1410204586
  • Abstract
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A report is presented over the occurrence of Hurler syndrome in a 20-year-old female with hereditary traits. The patient had already been diagnosed as buphthalmos at the age of 8 mon-ths and had underwent a glaucoma surgery at the age of 9 to each eye. Following findings have been worthy of note in the present pa-tient.

1. The amount of chondroitin sulfate B ex-creted in the urine has been very high and approximated about ten times the value in normal subjects.

2. Negative ERG and subnormal EOG findings were obtained.


Copyright © 1971, 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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