What is a MTHFR gene mutation?

Answer by  Veetzy (376)

Methylenetetrahydrofolate reductase (MTHFR) is a genetic mutation that inhibits the absorption of folic acid. Lack of folic acid in a pregnant woman results in an increased incidence of Downs Syndrome, Spina Bifida, neural tube defects or other congenital anomalies. Also, miscarriage and clotting disorders are not uncommon with this mutation.

Answer by  Loyola (378)

MTHFR is short 5,10-ethylenetetrahydrofolate reductase. This mutation prevents the production of enzymes needed to make amino acids, the building blocks of protein. The results are especially problematic for pregnancies.

Answer by  EmmaKitty (236)

MTHFR gene mutation is a rare genetic defect that causes pregnancy complications, such as miscarriage and chromosomal abnormalities (e. g. Downs Syndrome). The gene mutation inhibits folic acid absorption.