Ultrastructural and histochemical studies of a newly recognized form of systemic mucopolysaccharidosis. (Maroteaux-Lamy syndrome, mild phenotype)

Am J Ophthalmol. 1974 Jun;77(6):809-18. doi: 10.1016/0002-9394(74)90383-3.
No abstract available

MeSH terms

  • Adult
  • Basement Membrane / pathology
  • Biopsy
  • Chondroitin / metabolism*
  • Chondroitin / urine
  • Conjunctiva / pathology
  • Connective Tissue Cells
  • Cornea / pathology
  • Corneal Opacity / pathology*
  • Corneal Opacity / urine
  • Cytoplasm
  • Epithelial Cells
  • Fibroblasts
  • Glycosaminoglycans / urine
  • Histiocytes
  • Histocytochemistry
  • Humans
  • Inclusion Bodies
  • Joint Diseases / pathology
  • Male
  • Microscopy, Electron
  • Mucopolysaccharidoses / genetics
  • Mucopolysaccharidoses / pathology*
  • Mucopolysaccharidoses / urine
  • Phenotype
  • Plasma Cells
  • Retinitis Pigmentosa / pathology*
  • Retinitis Pigmentosa / urine
  • Schwann Cells
  • Syndrome

Substances

  • Glycosaminoglycans
  • Chondroitin