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Mucopolysaccharidosis III
Definition: Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme.

Synonym(s): Polydystrophic Oligophrenia / Sanfilippo's Syndrome / MPS III A / MPS III B / MPS III C / MPS III D / Mucopolysaccharidosis 3 / San Filippo's Syndrome / IIIs, Mucopolysaccharidosis / Mucopolysaccharidosis IIIs / Oligophrenia, Polydystrophic / Oligophrenias, Polydystrophic / Polydystrophic Oligophrenias / San Filippo Syndrome / San Filippos Syndrome / Sanfilippo Syndrome / Sanfilippos Syndrome / Syndrome, San Filippo's / Syndrome, Sanfilippo's
MeSH 2010 © U.S. National Library of Medicine®.
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  Web resources for "Mucopolysaccharidosis III"
             

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info: enter the site: (click below) domain of the site:  
view the robot description of the site Mucopolysaccharidosis III Symptoms, Diagnosis, Treatments and Causes - RightDiagnosis.comwww.wrongdiagnosis.com  
view the HON description of the site HONcode - Sanfilippo syndrome: MedlinePlus Medical Encyclopediawww.nlm.nih.gov  
view the HON description of the site HONcode - eye tracker - Opération myopie - Nantes - Correction myopie - Opération laser / lasik - Chirurgie myopiewww.operation-myopie.org  
view the HON description of the site HONcode - Medical Dictionary: MPS III - CureResearch.comwww.cureresearch.com  
view the HON description of the site HONcode - Orphanet: Sanfilippo syndrome type Awww.orpha.net 4
view the robot description of the site Ben's Dream - The Sanfilippo Research Foundationwww.bensdream.org  
 
 

Broader term(s): - Mucopolysaccharidoses - Metabolism, Inborn Errors - Genetic Diseases, Inborn - Congenital, Hereditary, and Neonatal Diseases and Abnormalities

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

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  Clinical Trials for "Mucopolysaccharidosis III"
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Broader term(s): - 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 

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

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