What is MTHFR disease

Normally, folic acid and other b vitamins break down homocysteine and.The most common variant in the mthfr gene is mthfr c677t.A deficiency in b9 can cause a growing fetus to develop devastating neural tube defects like spina bifida or anencephaly.This means at the 677 position in the mthfr gene, c is the expected dna base and t is the gene variant.Things that plague us, lyme and mthfr;

2 this variant may also be referred to as mthfr 677 c>t or mthfr 677 c→t.Similarly, you can have symptoms of mthfr.Mthfr tells our body how to create an enzyme involved in breaking down the amino acid homocysteine.Methylenetetrahydrofolate reductase deficiency is the most common genetic cause of elevated serum levels of homocysteine (hyperhomocysteinemia).it is caused by genetic defects in mthfr, which is an important enzyme in the methyl cycle.It is a key regulatory enzyme in the metabolism of folate.

Mthfr gene mutations have been found in medically reviewed studies to increase the risk factor of miscarriage and birth defects, including spina bifida.An mthfr gene is a genetic component of the folate cycle and is responsible for the conversion of folate from your diet and or supplements into an active form of folate that the body uses and needs as an essential nutrient, in other words, you can't live without it.Mthfr is at the top of a list of 16 genetic defects for autism.Learn about determining your mthfr status and getting treatment.Many rare diseases have limited information.

The mthfr mutation can stop this processing from occurring which can lead to problems and issues.Homocysteine is an amino acid that works to maintain the body's cells.Mthfr which is an enzyme needed for many different important processes in the body.Mthfr is a gene that acts somewhat like a light switch activating various body processes by either turning them on or off.