Hurler syndrome classification: Difference between revisions
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{{Hurler syndrome}} | {{Hurler syndrome}} | ||
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MPS I H or Hurler syndrome is the most severe of the MPS I subtypes. The other two types are MPS I S or [[Scheie syndrome]] and MPS I H-S or [[Hurler-Scheie syndrome]]. | ==Overview== | ||
MPS I is divided into three subtypes based on severity of symptoms. All three types result from an absence of, or insufficient levels of, the enzyme alpha-L-iduronidase. MPS I H or Hurler syndrome is the most severe of the MPS I subtypes. The other two types are MPS I S or [[Scheie syndrome]] and MPS I H-S or [[Hurler-Scheie syndrome]]. | |||
Hurler's Syndrome is often classified as a [[lysosomal storage disease]] and is mechanistically related to Hunter's Syndrome (X-linked recessive). | Hurler's Syndrome is often classified as a [[lysosomal storage disease]] and is mechanistically related to Hunter's Syndrome (X-linked recessive). | ||
==Classification== | |||
==References== | ==References== | ||
{{Reflist|2}} | |||
[[Category:Gastroenterology]] | |||
[[Category:Cardiology]] | |||
[[Category:Hepatology]] | |||
[[Category:Psychiatry]] | |||
[[Category:Metabolic disorders]] | |||
[[Category:Lysosomal storage diseases]] | |||
[[Category:Cardiology]] | |||
[[Category:Psychiatry]] | |||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category: | [[Category:Inborn errors of metabolism]] | ||
[[Category:needs content]] | |||
Latest revision as of 13:21, 19 July 2016
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Hurler syndrome classification On the Web |
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Risk calculators and risk factors for Hurler syndrome classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
MPS I is divided into three subtypes based on severity of symptoms. All three types result from an absence of, or insufficient levels of, the enzyme alpha-L-iduronidase. MPS I H or Hurler syndrome is the most severe of the MPS I subtypes. The other two types are MPS I S or Scheie syndrome and MPS I H-S or Hurler-Scheie syndrome.
Hurler's Syndrome is often classified as a lysosomal storage disease and is mechanistically related to Hunter's Syndrome (X-linked recessive).