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  1. Mucopolysaccharidosis Type I - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1162
    ... S, Wraith E, Guffon N. Attenuated type I mucopolysaccharidosis in the differential diagnosis of juvenile idiopathic arthritis: a series of 13 ... Giugliani R, Okuyama T, Wijburg F, Kaplan P. Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry. Eur ...
  2. Mucopolysaccharidosis Type III - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK546574
    ... Table 5. Genes of Interest in the Differential Diagnosis of Mucopolysaccharidosis Type III View in own window Gene Differential Diagnosis Disorder MOI Clinical Features of Differential Diagnosis Disorder ...
  3. Free Sialic Acid Storage Disorders - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1470
    ... Disease . Accessed 1-8-20 (Registration required). MPS = mucopolysaccharidosis Management Evaluations Following Initial Diagnosis To establish the extent of disease and needs ...
  4. Mucopolysaccharidosis type III: MedlinePlus Genetics 
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-iii
    ... Bodamer OA, Giugliani R, Wood T. The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): A changing landscape. Mol Genet ...
  5. Mucopolysaccharidosis type II: MedlinePlus Genetics 
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-ii
    ... Harmatz P, Munoz V, Muenzer J. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome). Pediatrics. 2008 Feb;121(2): ...
  6. IDS gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/ids
    ... Harmatz P, Munoz V, Muenzer J. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome). Pediatrics. 2008 Feb;121(2): ...
  7. Resource Bibliography - Enzyme-Replacement Therapies for Lysosomal Storage Diseases - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK117228
    ... Scarpa M, Almassy Z, Beck M, et al. Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease. Orphanet ...
  8. NLM Digital Collections - Proposal for a Genetics Research Center (pages 26-50) 
    Publication: Produced: 1 June 1973
    resource.nlm.nih.gov/101584906X17935
    ... C. B., “A Chemical Method for the Antenatal Diagnosis of Mucopolysaccharidoses." Lancet, 1, 83 (1970). 26c) Nadlec, H. L., ...
  9. NLM Digital Collections - Proposal for a Genetics Research Center 
    Publication: Produced: 1 June 1973
    resource.nlm.nih.gov/101584906X17932
    ... C. B., “A Chemical Method for the Antenatal Diagnosis of Mucopolysaccharidoses." Lancet, 1, 83 (1970). 26c) Nadlec, H. L., ...
  10. Mucopolysaccharidosis type IV: MedlinePlus Genetics 
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-iv
    ... abdomen (inguinal hernia). Unlike some other types of mucopolysaccharidosis, MPS IV does not affect intelligence. The life expectancy of individuals with MPS IV depends on the severity of symptoms. Severely affected individuals may survive only until late ...
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