Neonatal form of the hyperornithinaemia, hyperammonaemia, and homocitrullinuria (HHH) syndrome and prenatal diagnosis

Prenat Diagn. 1992 Sep;12(9):717-23. doi: 10.1002/pd.1970120905.
No abstract available

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / metabolism*
  • Ammonia / blood*
  • Cells, Cultured / metabolism
  • Citrulline / analogs & derivatives*
  • Citrulline / urine
  • Female
  • Gestational Age
  • Hepatitis B Surface Antigens / analysis
  • Humans
  • Hyaline Membrane Disease / pathology
  • Infant, Newborn
  • Male
  • Ornithine / blood*
  • Ornithine Carbamoyltransferase Deficiency Disease*
  • Ornithine-Oxo-Acid Transaminase / deficiency*
  • Pregnancy
  • Pregnancy Outcome
  • Prenatal Diagnosis
  • Syndrome

Substances

  • Hepatitis B Surface Antigens
  • homocitrulline
  • Citrulline
  • Ammonia
  • Ornithine
  • Ornithine-Oxo-Acid Transaminase