Moyamoya syndrome in a child with methyl tetrahydrofolate reductase mutation

Neurol India. 2017 Nov-Dec;65(6):1408-1409. doi: 10.4103/0028-3886.217935.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Brain / diagnostic imaging
  • Child
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Moyamoya Disease / diagnostic imaging
  • Moyamoya Disease / genetics*
  • Mutation

Substances

  • MTHFR protein, human
  • Methylenetetrahydrofolate Reductase (NADPH2)