Infantile sialic acid storage disease: report of the first case in South America

Clin Genet. 1999 May;55(5):386-7.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / pathology
  • Fatal Outcome
  • Female
  • Humans
  • Infant
  • Lysosomal Storage Diseases / metabolism
  • Lysosomal Storage Diseases / pathology*
  • N-Acetylneuraminic Acid / metabolism*

Substances

  • N-Acetylneuraminic Acid