Sepsis-like cerebrovascular event in a newborn with MTHFR homozygous mutation

Pediatr Int. 2010 Jun;52(3):499-500. doi: 10.1111/j.1442-200X.2010.03147.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Cerebrovascular Disorders / diagnosis
  • Cerebrovascular Disorders / genetics*
  • Electroencephalography
  • Follow-Up Studies
  • Gene Expression Regulation, Developmental
  • Genetic Predisposition to Disease*
  • Heterozygote
  • Homozygote
  • Humans
  • Infant, Newborn
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Mutation*
  • Pedigree
  • Seizures / diagnosis
  • Seizures / genetics*
  • Sepsis / complications
  • Sepsis / diagnosis*

Substances

  • Methylenetetrahydrofolate Reductase (NADPH2)