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Hierarchy  - English - French - German - Spanish - Portuguese - Italian - Dutch    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 / MeSH 2010 © U.S. National Library of Medicine®. Browse - New search

Web resources for "Mucopolysaccharidosis III" = Site with HON description   -   = Site with a robot description info: enter the site: (click below) domain of the site:   Mucopolysaccharidosis III Symptoms, Diagnosis, Treatments and Causes - RightDiagnosis.com www.wrongdiagnosis.com   HONcode - Sanfilippo syndrome: MedlinePlus Medical Encyclopedia www.nlm.nih.gov   HONcode - UCLA scientists reveal how deadly pediatric disorder develops in brain - UCLA Health and Medicine News www.uclahealth.org   HONcode - Medical Dictionary: MPS III - CureResearch.com www.cureresearch.com   HONcode - Orphanet: Sanfilippo syndrome type A www.orpha.net 4 Ben's Dream - The Sanfilippo Research Foundation www.bensdream.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 III" No results for this term. Browse other medical images in HONmedia? Browse - New search       Medical News for "Mucopolysaccharidosis III" No results for this term. More health news Browse - New search       Scientific articles from MEDLINE for "Mucopolysaccharidosis III"   - 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 III" ClinicalTrials.gov - Linking patients to medical research A Study of Patients With Sanfilippo Syndrome Type A (MPS IIIA) ALD-101 Adjuvant Therapy of Unrelated Umbilical Cord Blood Transfusion (UCBT) in Patients With Inherited Metabolic Diseases A Study of Patients With Sanfilippo Syndrome Type A (MPS IIIA) Broader term(s): - Mucopolysaccharidoses - Metabolism, Inborn Errors - Congenital, Hereditary, and Neonatal Diseases and Abnormalities Browse - New search       Medical Conferences/Events for "Mucopolysaccharidosis III" No results for this term. Consult HON's world-wide database of medical meetings Browse - New search       Refine the search for  "Mucopolysaccharidosis III" 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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