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Hierarchy  - English - French - German - Spanish - Portuguese - Italian - Dutch    Mucopolysaccharidosis VI Definition: Mucopolysaccharidosis with excessive chondroitin sulfate B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-acetylgalactosamine-4-sulfatase (arylsulfatase B). Synonym(s): Maroteaux-Lamy Syndrome / Polydystrophic Dwarfism / Mucopolysaccharidosis 6 / Dwarfism, Polydystrophic / MeSH 2010 © U.S. National Library of Medicine®. Browse - New search

Web resources for "Mucopolysaccharidosis VI" = Site with HON description   -   = Site with a robot description info: enter the site: (click below) domain of the site:   Mucopolysaccharidosis VI Symptoms, Diagnosis, Treatments and Causes - RightDiagnosis.com www.wrongdiagnosis.com   Whonamedit - Maroteaux-Lamy syndrome II www.whonamedit.com 3 Abstract | Mucopolysaccharidosis VI www.ojrd.com   rare-diseases — National Organization for Rare Disorders www.rarediseases.org   Broader term(s): - Mucopolysaccharidoses - Metabolism, Inborn Errors - Genetic Diseases, Inborn - Congenital, Hereditary, and Neonatal Diseases and Abnormalities Browse - New search       Medical image(s) for "Mucopolysaccharidosis VI" No results for this term. Browse other medical images in HONmedia? Browse - New search       Medical News for "Mucopolysaccharidosis VI" No results for this term. More health news Browse - New search       Scientific articles from MEDLINE for "Mucopolysaccharidosis VI"   - English - French - German - Spanish - Portuguese - Italian - Dutch     All recent articles  Therapy:  by recall    /  by precision  Diagnosis:  by recall    /  by precision  Etiology:  by recall    /  by precision  Prognosis:  by recall    /  by precision Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy Browse - New search       Clinical Trials for "Mucopolysaccharidosis VI" ClinicalTrials.gov - Linking patients to medical research A Phase 4 Two Dose Level Study of Naglazyme(TM) (Galsulfase) in Infants With MPS VI Mucopolysaccharidosis (MPS) VI Clinical Surveillance Program (CSP) Study of rhASB in Patients With Mucopolysaccharidosis VI Study of Recombinant Human N-Acetylgalactosamine 4-Sulfatase in Patients With MPS VI Open-Label Study of Efficacy and Safety of Recombinant Human N-acetylgalactosamine 4-sulfatase in Patients With MPS VI Stem Cell Transplantation for Hurler   More results Broader term(s): - Mucopolysaccharidoses - Metabolism, Inborn Errors - Congenital, Hereditary, and Neonatal Diseases and Abnormalities Browse - New search       Medical Conferences/Events for "Mucopolysaccharidosis VI" No results for this term. Consult HON's world-wide database of medical meetings Browse - New search       Refine the search for  "Mucopolysaccharidosis VI" 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®. Browse - New search

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