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Journal of Inherited Metabolic Disease

, Volume 32, Issue 4, pp 582–583 | Cite as

Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype

  • Y. Suzuki
  • A. Aoyama
  • T. Kato
  • N. Shimozawa
  • T. Orii
IMAGES IN METABOLIC MEDICINE

Keywords

Retinitis Pigmentosa Dermatan Sulfate Arylsulfatase Mucopolysaccharidosis Hunter Syndrome 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Ashworth JL, Biswas S, Wraith E, Lloyd IC. Mucopolysaccharidosis and the eye. Surv Ophthalmol 2006:51: 1–17. doi: 10.1016/j.survophthal.2005.11.007 PubMedCrossRefGoogle Scholar
  2. Young ID, Harper PS. Mild form of Hunter syndrome: clinical delineation based on 31 cases. Arch Dis Child 1982;57: 828–836. doi: 10.1136/adc.57.11.828 PubMedCrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2009

Authors and Affiliations

  • Y. Suzuki
    • 1
  • A. Aoyama
    • 2
  • T. Kato
    • 1
  • N. Shimozawa
    • 3
  • T. Orii
    • 4
  1. 1.Department of Pediatrics and Medical Education Development CenterGifu University Graduate School of MedicineGifuJapan
  2. 2.Department of OphthalmologyGifu University Graduate School of MedicineGifuJapan
  3. 3.Division of Genomic Research, Life Science Research CenterGifu UniversityGifuJapan
  4. 4.Orii ClinicGifuJapan

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