Mucopolysaccharidosis (MPS): classification

Evidence-based neurology checklist on mucopolysaccharidosis (mps): classification: Types of MPS MPS I: Hurler-Scheie disease MPS I: Hurler disease: severe infantile or childhood onset MPS I: Scheie disease: milder later or adult onset MPS II: Hunter disease MPS III A-E: Sanfilippo disease MPS IV A…

Types of MPS

  • MPS I: Hurler-Scheie disease
  • MPS I: Hurler disease: severe infantile or childhood onset
  • MPS I: Scheie disease: milder later or adult onset
  • MPS II: Hunter disease
  • MPS III A-E: Sanfilippo disease
  • MPS IV A and B: Morquio disease
  • MPS V: Now Scheie disease
  • MPS VI: Maroteaux-Lamy disease
  • MPS VII: Sly disease
  • MPS IX: Hyaluronidase deficiency
  • MPS X
  • MPSPS: MPS plus syndrome

References

  1. Lehman TJ, Miller N, Norquist B, Underhill L, Keutzer J. Diagnosis of the mucopolysaccharidoses. Rheumatology (Oxford) 2011; 50(Suppl 5):v41-v48. 
  2. Muenzer J. Overview of the mucopolysaccharidoses. Rheumatology 2011; 50:v4-v12.
  3. Wiśniewska K, Wolski J, Gaffke L, Cyske Z, Pierzynowska K, Węgrzyn G. Misdiagnosis in mucopolysaccharidoses. J Appl Genet 2022; 63:475-495.

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