The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK

The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK

<p>Abstract</p> <p>Background</p> <p>Mucopolysaccharidosis type I (MPS I) is a rare lysosomal storage disease subdivided into three phenotypes of increasing severity: Scheie, Hurler-Scheie and Hurler. To gauge the effectiveness of treatments and to determine the load li...

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Bibliographic Details
Main Authors: Moore David, Connock Martin J, Wraith Ed, Lavery Christine
Format: Article
Language:English
Published: BMC 2008-09-01
Series:Orphanet Journal of Rare Diseases
Online Access:http://www.ojrd.com/content/3/1/24

Internet

http://www.ojrd.com/content/3/1/24

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