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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2008-9-29
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pubmed:abstractText |
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 likely to fall on health-care systems, it is necessary to understand the prevalence and natural progression of the disease especially with regard to life-expectancy. In general such data on the natural history of lysosomal storage diseases is sparse.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-10480370,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-14608657,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-16254305,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-16254306,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-16435194,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-17030825,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-17336562,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-17529997,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-17606547,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-2118475,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-4250044,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-9439667,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-9610798,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18796143-9918480
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
1750-1172
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
24
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:18796143-Adolescent,
pubmed-meshheading:18796143-Adult,
pubmed-meshheading:18796143-Child,
pubmed-meshheading:18796143-Demography,
pubmed-meshheading:18796143-England,
pubmed-meshheading:18796143-Humans,
pubmed-meshheading:18796143-Kaplan-Meier Estimate,
pubmed-meshheading:18796143-Mucopolysaccharidosis I,
pubmed-meshheading:18796143-Phenotype,
pubmed-meshheading:18796143-Prevalence,
pubmed-meshheading:18796143-Registries,
pubmed-meshheading:18796143-Societies, Medical,
pubmed-meshheading:18796143-Wales
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pubmed:year |
2008
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pubmed:articleTitle |
The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK.
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pubmed:affiliation |
Department of Public Health and Epidemiology, University of Birmingham, Birmingham, UK. d.j.moore@bham.ac.uk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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