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Mucopolysaccharidosis II
Definition: Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.

Synonym(s): Gargoylism, Hunter Syndrome / Hunter's Syndrome / Hunter Syndrome Gargoylism / Mucopolysaccharidosis 2 / Gargoylisms, Hunter Syndrome / Hunter Syndrome / Hunter Syndrome Gargoylisms / Hunters Syndrome / IIs, Mucopolysaccharidosis / Mucopolysaccharidosis IIs / Syndrome, Hunter's
See also:
Mucopolysaccharidosis I   

MeSH 2010 © U.S. National Library of Medicine®.
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  Web resources for "Mucopolysaccharidosis II"
             

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view the robot description of the site Mucopolysaccharidosis II Symptoms, Diagnosis, Treatments and Causes - RightDiagnosis.comwww.wrongdiagnosis.com 2
view the HON description of the site HONcode - Medical Dictionary: Hunter syndrome - CureResearch.comwww.cureresearch.com  
view the HON description of the site HONcode - Hunter syndrome: MedlinePlus Medical Encyclopediawww.nlm.nih.gov  
view the robot description of the site rare-diseases — National Organization for Rare Disorderswww.rarediseases.org  
view the robot description of the site Elaprase Side Effects, Uses, & Interactionswww.drugwatch.com  
view the robot description of the site Whonamedit - Hunter's syndrome (Charles A. Hunter)www.whonamedit.com  
view the robot description of the site Mucopolysaccharidoses Fact Sheet: National Institute of Neurological Disorders and Stroke (NINDS)www.ninds.nih.gov 4
 
 

See also: - Mucopolysaccharidosis I

Broader term(s): - Mental Retardation, X-Linked - Mental Retardation - Neurobehavioral Manifestations - Neurologic Manifestations - Nervous System Diseases - Mucopolysaccharidoses - Metabolism, Inborn Errors - Genetic Diseases, Inborn - Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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See also: - Mucopolysaccharidosis I
Broader term(s): - Nervous System Diseases
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  Medical News for "Mucopolysaccharidosis II"
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Broader term(s): - Mental Retardation - Nervous System Diseases

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  Scientific articles from MEDLINE for "Mucopolysaccharidosis II"
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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy

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  Clinical Trials for "Mucopolysaccharidosis II"
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See also: - Mucopolysaccharidosis I

Broader term(s): - Mental Retardation - Neurobehavioral Manifestations - Neurologic Manifestations - Nervous System Diseases - Mucopolysaccharidoses - Metabolism, Inborn Errors - Congenital, Hereditary, and Neonatal Diseases and Abnormalities

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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy


  Broader term(s):
      Diseases
          Nutritional and Metabolic Diseases
              Metabolic Diseases
                  Metabolism, Inborn Errors
                      Lysosomal Storage Diseases
                          Mucopolysaccharidoses 
                      Carbohydrate Metabolism, Inborn Errors
                          Mucopolysaccharidoses 
      Diseases
          Skin and Connective Tissue Diseases
              Connective Tissue Diseases
                  Mucinoses
                      Mucopolysaccharidoses 
      Diseases
          Congenital, Hereditary, and Neonatal Diseases and Abnormalities
              Genetic Diseases, Inborn
                  Metabolism, Inborn Errors
                      Lysosomal Storage Diseases
                          Mucopolysaccharidoses 
                      Carbohydrate Metabolism, Inborn Errors
                          Mucopolysaccharidoses 
                  Heredodegenerative Disorders, Nervous System
                      Mental Retardation, X-Linked 
      Diseases
          Congenital, Hereditary, and Neonatal Diseases and Abnormalities
              Genetic Diseases, Inborn
                  Genetic Diseases, X-Linked
                      Mental Retardation, X-Linked 
      Diseases
          Nervous System Diseases
              Neurologic Manifestations
                  Neurobehavioral Manifestations
                      Mental Retardation
                          Mental Retardation, X-Linked 

MeSH 2010 © U.S. National Library of Medicine®.

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