Congenital disorder of glycosylation type Ia revealed by hypertransaminasemia and failure to thrive in a young boy with normal neurodevelopment

J Pediatr Gastroenterol Nutr. 2005 Feb;40(2):230-2. doi: 10.1097/00005176-200502000-00030.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • Failure to Thrive / blood
  • Failure to Thrive / etiology
  • Glycosylation
  • Humans
  • Male
  • Metabolism, Inborn Errors / blood
  • Metabolism, Inborn Errors / complications
  • Metabolism, Inborn Errors / genetics*
  • Nervous System Diseases / etiology*
  • Transaminases / blood*

Substances

  • Transaminases