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Results 1 - 9 of 9 for "Mucopolysaccharidosis," "MPS-II"
  1. ... 2-sulfatase deficiency MPS II Genetic Testing Registry: Mucopolysaccharidosis, MPS-II Mucopolysaccharidosis type II Disease InfoSearch National Organization for ...
  2. Mucopolysaccharidosis type II (MPS II) is a rare disease in which the body is missing or does not have enough of ... More information and support for people with MPS II and their families can be found at: National MPS Society -- mpssociety.org/ ...
  3. ... the IDS gene have been found to cause mucopolysaccharidosis type II (MPS II). Variants that change one DNA building block (nucleotide) ... Munoz V, Muenzer J. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome). Pediatrics. 2008 Feb;121(2):e377- ...
  4. Mucopolysaccharidoses From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Carbohydrate Metabolism Disorders/Specifics ... Carbohydrate Metabolism Disorders ... From the National Institutes of Health ... National Institute of Neurological Disorders ...
  5. ... I (Hurler syndrome; Hurler-Scheie syndrome; Scheie syndrome) MPS II (Hunter syndrome) MPS III (Sanfilippo syndrome)
  6. ... There are several other types of MPSs, including: MPS II (Hunter syndrome) MPS III (Sanfilippo syndrome) MPS IV (Morquio syndrome)
  7. ... I (Hurler syndrome; Hurler-Scheie syndrome; Scheie syndrome) MPS II (Hunter syndrome) MPS III (Sanfilippo syndrome) MPS IV (Morquio syndrome)
  8. ... I (Hurler syndrome; Hurler-Scheie syndrome; Scheie syndrome) MPS II (Hunter syndrome) MPS IV (Morquio syndrome)
  9. ... and Hurler/Scheie syndromes (MPS I), Hunter syndrome (MPS II), ... may have a symptom or family history of one of these disorders.