Methylene Tetrahydrofolate Reductase Deficiency

Indian J Pediatr. 2020 Nov;87(11):951-953. doi: 10.1007/s12098-020-03290-3. Epub 2020 May 26.

Abstract

5,10-Methylene-tetrahydrofolate reductase (MTHFR) deficiency is a rare, autosomal recessive, metabolic disorder of folate metabolism, which affects homocysteine remethylation. Elevated homocysteine with normal or low methionine level is the key to diagnosis. Early recognition and treatment with betaine, has been shown to improve the survival and neurological outcomes. The authors report five Indian patients from three unrelated families, with MTHFR deficiency to emphasize the importance of early recognition and initiation of specific treatment.

Keywords: Betaine; Homocysteine; Methylene tetrahydrofolate reductase deficiency.

MeSH terms

  • Folic Acid
  • Homocysteine
  • Homocystinuria* / diagnosis
  • Homocystinuria* / genetics
  • Humans
  • Methylenetetrahydrofolate Reductase (NADPH2) / deficiency
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics
  • Muscle Spasticity
  • Psychotic Disorders*

Substances

  • Homocysteine
  • Folic Acid
  • Methylenetetrahydrofolate Reductase (NADPH2)

Supplementary concepts

  • Methylenetetrahydrofolate reductase deficiency