Intracranial haemorrhage in siblings and ornithine transcarbamylase deficiency

Acta Paediatr Scand. 1982 Jul;71(4):671-3. doi: 10.1111/j.1651-2227.1982.tb09497.x.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / genetics*
  • Ammonia / blood*
  • Cerebral Hemorrhage / genetics*
  • Humans
  • Infant, Newborn
  • Infant, Newborn, Diseases*
  • Male
  • Ornithine Carbamoyltransferase Deficiency Disease*

Substances

  • Ammonia