A new type of idiopathic hyperglycinemia with hypo-oxaluria

Pediatrics. 1965 Dec;36(6):882-91.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Metabolism, Inborn Errors*
  • Blood
  • Cerebrospinal Fluid
  • Child, Preschool
  • Chromatography
  • Glycine / metabolism*
  • Humans
  • Infant
  • Intellectual Disability / etiology
  • Male
  • Oxalates / metabolism*
  • Sweat
  • Urine

Substances

  • Oxalates
  • Glycine