Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset

J Neurol Neurosurg Psychiatry. 1996 Jan;60(1):107-8. doi: 10.1136/jnnp.60.1.107.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Child
  • Female
  • Homocystinuria / complications*
  • Homocystinuria / enzymology
  • Homocystinuria / genetics*
  • Humans
  • Metabolism, Inborn Errors / complications*
  • Metabolism, Inborn Errors / enzymology
  • Metabolism, Inborn Errors / genetics*
  • Methylmalonic Acid / metabolism*
  • Vitamin B 12 / metabolism*

Substances

  • Methylmalonic Acid
  • Vitamin B 12