Skip to main content
SpringerLink
Log in

Pseudodeficiency of α-iduronidase

  • Case Report
  • Published:
Journal of Inherited Metabolic Disease

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  • Gatti R, Borrone C, Filocamo M, Pannone N, DiNatale P (1985) Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cells.Prenat Diagn 5: 149–154.

    Google Scholar 

  • Whitley CB, Gorlin RJ, Krivit W (1987) A nonpathologic allele (IW) for low α-L-iduronidase enzyme activityvis-à-vis prenatal diagnosis of Hurler syndrome.Am J Med Genet 28: 233–243.

    Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Greenwood Genetic Center, 1 Gregor Mendel Circle, 29646, Greenwood, SC, USA

    H. A. Taylor

  2. Kennedy Krieger Institute, 707 North Broadway, 21205, Baltimore, MD, USA

    G. H. Thomas

Authors
  1. H. A. Taylor
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. G. H. Thomas
    View author publications

    You can also search for this author in PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Taylor, H.A., Thomas, G.H. Pseudodeficiency of α-iduronidase. J Inherit Metab Dis 16, 1058–1059 (1993). https://doi.org/10.1007/BF00711533

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00711533

Keywords

Search

Navigation